Tag: M.W:100-200

Application of 2927-71-1, With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.2927-71-1, name is 2,4-Dichloro-5-fluoropyrimidine, molecular formula is C4HCl2FN2, molecular weight is 166.9685, as common compound, the synthetic route is as follows.

Under a nitrogen atmosphere, 60 2,4-dichloro-5-fluoropyrimidine (517 mg, 3.1 mmol), 61 sodium carbonate (583 mg, 5.5 mmol) was dissolved in a mixed solution of 1 mL 48 water and 5 mL 62 ethylene glycol dimethyl ether, 63 PdCl2(PPh3)2 (4.7 mg, 66 mumol) was added, heated to 80 C., and then a solution of 64 4-fluoro-1-isopropyl-2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-1H-benzo[d]imidazole (700 mg, 2.2 mmol) in ethylene glycol dimethyl ether (40 mL) was added, stirred at this temperature for 4 hours, and then 30 mL water was added, stirring was continued for 25 minutes, filtered and dired the filter cake at 80 C. and then washed with isopropyl alcohol, the product 65 6-(2-chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole 425 mg was obtained after drying, yield: 60%. LC-MS(APCI): m/z=322.7 (M+1).

The chemical industry reduces the impact on the environment during synthesis 2927-71-1, I believe this compound will play a more active role in future production and life.

Reference:
Patent; Shenzhen TargetRx, Inc.; Wang, Yihan; Ren, Xingye; Jin, Jian; Li, Huanyin; Ai, Yixin; (162 pag.)US2019/152954; (2019); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Electric Literature of 3680-69-1 ,Some common heterocyclic compound, 3680-69-1, molecular formula is C6H4ClN3, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

A typical procedure for the preparation of 3a:2-bromopropane (74 mg, 0.6 mmol) was added to a solution of 1a (92 mg, 0.6 mmol) and K2CO3 (110 mg, 0.8 mmol) in 5 mL DMF at 70 C. According to TLC the reaction went to completion after 4 h. The mixture was extracted with ethyl acetate (3 * 10 mL). The combined organic layers were washed with brine(10 mL), dried over anhydrous Na2SO4, filtered and concentrated to give the crude product 2a, which was added to a solution of amino-phenol(66 mg, 0.6 mmol) and Cs2CO3 (585 mg, 1.8 mmol) in 10 mL DMSO without further purification. After stirring for 6 h at 80 C, the mixture was cooled to room temperature and extracted with ethyl acetate (3 * 10 mL). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was further purified by column chromatography(petroleum ether/ethyl acetate 2:1) to afford compound 3a as a brown solid(121 mg, 75% over two steps).

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 3680-69-1, 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine, other downstream synthetic routes, hurry up and to see.

Reference:
Article; Liu, Yang; Fang, Jianping; Cai, Haiyan; Xiao, Fei; Ding, Kan; Hu, Youhong; Bioorganic and Medicinal Chemistry; vol. 20; 18; (2012); p. 5473 – 5482;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 3993-78-0, name is 2-Amino-4-chloropyrimidine, the common compound, a new synthetic route is introduced below. Formula: C4H4ClN3

[0879] To a mixture of 2-amino-4-chloro-pyrimidine 79 (10.2 g, 79 mmol) in methanol (140 mL) and acetonitrile (100 mL), N-bromosuccinimide (14.01 g, 79 mmol) was added, and the resulting mixture was stirred at RT for about 0.5 h. The reaction mixture was treated with Et2O (200 mL), then cooled to about 5 C. and stirred for about 1 h. The mixture was filtered and the product air dried to afford compound 134.

The synthetic route of 3993-78-0 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; INTELLKINE, LLC; INFINITY PHARMACEUTICALS, INC.; CASTRO, Alfredo C.; EVANS, Catherine A.; JANARDANANNAIR, Somarajannair; LESCARBEAU, Andre; LIU, Tao; SNYDER, Daniel A.; TREMBLAY, Martin R.; REN, Pingda; LIU, Yi; LI, Liansheng; CHAN, Katrina; US2013/53362; (2013); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Synthetic Route of 10070-92-5 ,Some common heterocyclic compound, 10070-92-5, molecular formula is C5H4N2O, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

To a solution of pyrimidine-5-carbaldehyde (0.300 g, 2.77 mmol) in methanol (6 mL), sodium borohydride (0.158g, 4.16 mmol) was added at 0 C over 10 minutes and the reaction mixture was stirred at the same temperature for 30 min. After completion of the reaction, the solvent was removed under vacuum. The residue obtained was poured into water (30 mL), extracted with ethyl acetate (150 mL), The organic layer was dried over sodium sulfate and concentrated to provide the title compound (0.160 g, 52.4%), 1H NMR (400 MHz, DMSO-d6) delta ppm 9.18-9.20 (s, 1H), 8.74 (s, 2H), 5.49-5.67 (b, 1H), 4.60 (s, 2H).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,10070-92-5, its application will become more common.

Reference:
Patent; TEMPERO PHARMACEUTICALS, INC.; BALOGLU, Erkan; GHOSH, Shomir; LOBERA, Mercedes; SCHMIDT, Darby, R.; WO2013/19621; (2013); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Related Products of 7461-50-9, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 7461-50-9, name is 2-Chloropyrimidin-4-amine. A new synthetic method of this compound is introduced below.

To a reaction vessel was added 2-chloropyrimidin-4-amine (1.0 g, 8.0 mmol, 1.1 equiv), 3,3- dimethylpiperidin-4-ol (1.0 g, 9.0 mmol, 1.0 equiv), triethylamine (3.0 g, 30 mmol, 4.0 equiv), and 2-propanol (5 mL). The sealed reaction vessel was heated under microwave irradiation at 150 C for 45 min. The reaction mixture was cooled to room temperature, diluted with saturated aqueous sodium bicarbonate and extracted with dichloromethane. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo to afford l-(4-aminopyrimidin-2-yl)-3,3- dimethyl-piperdin-4-ol (1.24 g, 70%). LCMS (ESI): [M+H]+ = 223.2; lH NMR (300 MHz, DMSO-d6) delta 7.69 (d, J= 5.6 Hz, 1H), 6.28 (s, 2H), 5.64 (d, J= 5.6 Hz, 1H), 4.55 (d, J= 4.7 Hz, 1H), 4.33 – 4.22 (m, 1H), 4.02 (dd, J= 12.8, 1.7 Hz, 1H), 3.25 (dd, J= 9.4, 4.6 Hz, 1H), 3.08 – 2.96 (m, 1H), 2.75 (d, J= 13.0 Hz, 1H), 1.66 – 1.54 (m, 1H), 1.47 – 1.35 (m, 1H), 0.87 (s, 3H), 0.74 (s, 3 H).

At the same time, in my other blogs, there are other synthetic methods of this type of compound,7461-50-9, 2-Chloropyrimidin-4-amine, and friends who are interested can also refer to it.

Reference:
Patent; GENENTECH, INC.; BRYAN, Marian C.; CHAN, Bryan; DIEDERICH, Francois; DOTSON, Jennafer; HANAN, Emily; HEFFRON, Timothy; LAINCHBURY, Michael; HEALD, Robert; SEWARD, Eileen M.; WO2014/210354; (2014); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Reference of 36315-01-2, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 36315-01-2, name is 2-Amino-4,6-dimethoxypyrimidine. A new synthetic method of this compound is introduced below.

In a 1 OOO mL reaction flask, 100 g of 2-sulfonyl chloride-N, N-dimethylnicotinamide (0.40 mol) 40 g of sodium cyanate (0.62 mol), 101 g of triethylamine (1.00 mol) and 125 g of acetonitrile were charged and the mixture was stirred at 25 ± 5 C for isocyanating. After 5 h, 75 g of 2-amino-4,6-dimethoxypyrimidine (0.48 mol) was added to the reaction flask and stirred for 1 h at ambient temperature (0 to 40 C). After the completion of the condensation reaction, 500 g of deionized water (about 1.5 h) was added dropwise to the reaction bottle. After dropping, the pH was adjusted to 1.0 with hydrochloric acid, After drying, 157.8 g of nicosulfuron were obtained in a yield of 92.1% and a purity of 95.7%.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,36315-01-2, 2-Amino-4,6-dimethoxypyrimidine, and friends who are interested can also refer to it.

Reference:
Patent; Jiangsu agricultural hormone Engineering Technology Research Center Co., Ltd.; Jiangsu Hormone Research Institute Co., Ltd; Sun, Yong Hui; kong, Fan Lei; Shi, yueping; Gao, Jian Hong; Zhang, Yuan yuan; Cao, Wei; (5 pag.)CN103524493; (2016); B;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Application of 932-52-5 ,Some common heterocyclic compound, 932-52-5, molecular formula is C4H5N3O2, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

7 g of caustic soda (0.175 mol) diluted in 350 ml of water were added to 21.5 g of 5-aminouracil (0.17 mol). The mixture was heated at a boiling water bath until 5-aminouracil was fully dissolved. Then 32 g of 3,5-dichlorosalicylic aldehyde (0.17 mol) dissolved in 150 ml of hot ethanol were added in portions to the reaction mass at the temperature of the boiling water bath while stirring. For the purpose of quantitative transfer of aldehyde into the reaction flask, the vessel in which it was dissolved was washed with 50 ml of ethanol. A sediment of orange-red color precipitated in the flask. Then the reaction mass was stirred for 30 more minutes at the water bath and was gradually cooled down to room temperature. The obtained residue was filtered, washed with 300 ml of ethanol and dried. 600 ml of aqueous ethanol were distilled off the filtrate by means of rotary evaporator. The remaining mixture was filtered by means of glass filter to obtain 75.5 g of the target compound.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 932-52-5, 5-Aminopyrimidine-2,4(1H,3H)-dione, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Tets, Viktor Veniaminovich; Tets, Georgy Viktorovich; Krutikov, Viktor Iosifovich; US2013/261301; (2013); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 3993-78-0, name is 2-Amino-4-chloropyrimidine, the common compound, a new synthetic route is introduced below. Product Details of 3993-78-0

NaH (1.15 g, 60% in mineral oil, 28.7 mmol) was added the mixture of 4-chloropyrimidin-2-amine (1.0 g, 7.75 mmol) and solketal (3.07 g, 23.25 mmol) in dioxane (12 mL) solution at 0 C. The temperature was elevated to 120 C for 15 h. After cooling to room temp, the solids were filtered, filtrate was concentrated and residue purified by column chromatography to give 4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)pyrimidin-2- amine (1.2 g, 69 %). MS (ESI) calcd for C10H15N3O3: 225.11

The synthetic route of 3993-78-0 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; SIRTRIS PHARMACEUTICALS, INC.; CASAUBON, Rebecca, L.; NARAYAN, Radha; OALMANN, Christopher; VU, Chi, B.; WO2013/59587; (2013); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.69034-12-4, name is 2-Chloro-5-(trifluoromethyl)pyrimidine, molecular formula is C5H2ClF3N2, molecular weight is 182.531, as common compound, the synthetic route is as follows.Recommanded Product: 2-Chloro-5-(trifluoromethyl)pyrimidine

A mixture of l-((lr,4r)-4-((2-fluoro-4- (methylsulfonyl)phenoxy)methyl)cyclohexyl)piperazine dihydrochloride (29 mg, 0.065 mmol), 2-chloro-5-(trifluoromethyl)pyrimidine (16 mg, 0.085 mmol) and triethylamine (34 mu, 0.262 mmol) in IPA (1.5 mL) was heated at 130 C for 40 min under microwave irradiation. The mixture was cooled down. The solid precipitate was collected, washed with IPA and dried to give the title compound (30 mg, 89.2%). Exact mass calculated for C23H28F4N4O3S: 516.2, found: LCMS m/z = 517.2 [M+H]+; lU NMR (400 MHz, CDC13) delta ppm 1.10-1.20 (m, 2H),1.35-1.45 (m, 2H), 1.78-1.90 (m, 1H), 1.98-2.10 (m, 4H), 2.40-2.50 (m, 1H), 2.65-2.75 (m, 4H), 3.03 (s, 3H), 3.85-4.05 (m, 4H), 3.90 (d, J = 6.2 Hz, 2H), 7.05 (t, J = 8.0 Hz, 1H), 7.62-7.69 (m, 2H), 8.49 (s, 2H).

At the same time, in my other blogs, there are other synthetic methods of this type of compound,69034-12-4, 2-Chloro-5-(trifluoromethyl)pyrimidine, and friends who are interested can also refer to it.

Reference:
Patent; ARENA PHARMACEUTICALS, INC.; JONES, Robert M.; BUZARD, Daniel J.; HAN, Sangdon; KIM, Sun Hee; LEHMANN, Juerg; YUE, Dawei; ZHU, Xiuwen; WO2012/145361; (2012); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 3934-20-1, name is 2,4-Dichloropyrimidine. This compound has unique chemical properties. The synthetic route is as follows. Application In Synthesis of 2,4-Dichloropyrimidine

General procedure: A mixture of 2,4-dichloropyrimidine (6.71 mmol), ary-boronic acid (6.71 mmol). DMF or dioxane (10 ml) was added to the above mixture followed by aqueous sodium carbonate (2 M, 6 ml,). The reaction mixture was degassed with argon for 15 min. Pd(PPh3)4 (50 mg, 0.17 mmol) was added and again degassed 5 min. The reaction mixture was maintained at rt for 12 h. The mixture was subsequently filtered and the remaining solid was washed with EtOAc. The filtrate was washed again with water and brine. The organic layer was separated, dried with anhydrous Na2SO4 and filtered. The organic layer was purified by silica gel column chromatography to give the desired product.

With the rapid development of chemical substances, we look forward to future research findings about 3934-20-1.

Reference:
Article; Toviwek, Borvornwat; Suphakun, Praphasri; Choowongkomon, Kiattawee; Hannongbua, Supa; Gleeson, M. Paul; Bioorganic and Medicinal Chemistry Letters; vol. 27; 20; (2017); p. 4749 – 4754;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia