Bromides-buliding-blocks

937046-98-5, Name is 7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine, 937046-98-5, belongs to bromides-buliding-blocks compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows.

To a 500 ml jacketed 3-necked flask fitted with a thermocouple, vacuum/No inlet and overhead stirring apparatus was added 7-bromo-pyrrolo[2,l -f][1,2,4]triazin- 4-ylamine (20g, 1.0 equiv., 94 mraol). This was suspended in dry THF (200 ml) and cooled to 0 C. To this was added dropwise 31 ml of MeMgCl solution (3M in THF, 1.0 equiv.). This proceeded with bubbling and a significant exotherm. The rate of addition was controlled to maintain internal temperature below 10 C. Following completion of addition and cooling to 0 C, 1,2-bis(chlorodimethyIsilyl)ethane (20.2 g, 1.0 equiv.) was added in a single portion, with exotherm to about 5 C. Once the temperature had returned to 0 C, a second portion of 31 ml MeMgCl (3M in THF, 1.0 equiv.) was added as before. Once the temperature returned to 0 C, 80 ml of iPrMgCl-LiCl solution (1.3 M in THF, 1.1 equiv.) was added. The resulting dark solution was allowed to warm to room temperature, and conversion was checked by HPLC, with sample preparation in MeOH to provide the des-bromo heterocycle. Once the conversion of 7-bromo-pyrrolo[2,l-f][1,2,4]triazin-4-yIamine was >95% complete (5 hrs), the solution was cooled to 0 C, and a solution of 2b (40.6 g, 94 mraol) in 100 ml THF was added via canulla. The resulting orange solution was allowed to warm to room temperature and stirred overnight. After 12 hrs, the reaction was found to be complete by HPLC (sample prepared in H20/MeCN 1 :1). At this point 200 ml of 13% NH4CI solution was added and briskly stirred for 15 min. After this time, agitation was ceased, and the two layers were allowed to separate. The organic layer was then reduced to roughly 70 ml, and MeCN (100 ml) was added, followed by 300 ml 1M aqueous C1 solution. The resulting slurry was stirred at room temperature for 2 hrs, then filtered through a sintered glass funnel. The resulting solid was dried overnight under vacuum at 45 C to give 2c. Yield 37.6 g (66%)

Statistics shows that 7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine is playing an increasingly important role. we look forward to future research findings about 937046-98-5.

Reference:
Patent; GILEAD SCIENCES, INC.; BUTLER, Thomas; CHO, Aesop; GRAETZ, Benjamin, R.; KIM, Choung, U.; METOBO, Samuel, E.; SAUNDERS, Oliver, L.; WALTMAN, Andrew, W.; XU, Jie; ZHANG, Lijun; WO2011/35250; (2011); A1;,
Bromide – Wikipedia,
bromide – Wiktionary

In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 2695-47-8 as follows. 2695-47-8

Sodium hydride (60% dispersion in mineral oil, 31.5 g, 1.28 eq.) was slowly added under nitrogen atmosphere to a solution of Lambda/-methyl-2,2,2-trifluoroacetamide (100 g, 1.28 eq.) in DMF (500 mL) at 0 0C. The reaction mixture was stirred for 90 min at 0 0C, and then 6-bromo-l-hexene (100 g, 1 eq.) was added dropwise over 45 min. The reaction mixture was allowed to warm up to room temperature, and stirred for 3 days at room temperature. The reaction mixture was then poured into water and extracted tree time with EtOAc. The combined organics layers were dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel to produce compound 31A as colorless oil in 56% yield. 1U NMR (DMSO-J6, 400 MHz) delta 1.27-1.38 (m, 2H), 1.48-1.60 (m, 2H), 2.00-2.06 (m, 2H), 2.93-3.07(2m, 3H), 3.35-3.40 (m, 2H), 4.92- 5.04 (m, 2H), 5.73-5.83 (m, IH).

According to the analysis of related databases, 2695-47-8, the application of this compound in the production field has become more and more popular.

Reference:
Patent; IDENIX PHARMACEUTICALS, INC.; PARSY, Christophe Claude; ALEXANDRE, Francois-Rene; LEROY, Frederic; CONVARD, Thierry; SURLERAUX, Dominique; WO2011/17389; (2011); A1;,
Bromide – Wikipedia,
bromide – Wiktionary

1435-53-6, The chemical industry reduces the impact on the environment during synthesis 1435-53-6, name is 2,4-Dibromo-1-fluorobenzene, I believe this compound will play a more active role in future production and life.

The 1L in three-mouth bottle, by adding benzo [d] imidazole (11.8g, 0 . 1mol), 2, 4-dibromide fluoride bonzene (51g, 0.2mol), Cs 2 CO 3 (65g, 0.2mol), N, N-dimethyl acetamide (DMA, 350g), N 2 protection, warming to reflux, thermal insulation reaction 48h, to room temperature, the reaction solution slowly into 1.4L deionized water, stirring 30 min, filtered, 400mLX2 deionized water washing, the crude product by silica gel column chromatography, eluting agent is petroleum ether: ethyl acetate = 2:1, to obtain the target compound 1-(2, 4-dibromo) phenyl-benzo [d] imidazole (compound 1a) 25.7g, yield 73%,

The chemical industry reduces the impact on the environment during synthesis 2,4-Dibromo-1-fluorobenzene. I believe this compound will play a more active role in future production and life.

Reference:
Patent; The energy-Mason Co.; Sheng, Lei; Shi, Yu; Zhang, Xinxin; Gao, Ziliang; Zhang, Xueheng; Guo, Haiyan; (31 pag.)CN104109532; (2016); B;,
Bromide – Wikipedia,
bromide – Wiktionary

A common compound: 67567-26-4, name is 4-Bromo-2,6-difluoroaniline, belongs to bromides-buliding-blocks compound, it can change the direction of chemical reaction, and react with certain compounds to generate new functional products. A new synthetic method of this compound is introduced below. 67567-26-4

Step 1: Preparation of N-(4-bromo-2,6-difluorophenyl)-4-chlorobutanamide. [0804] To a solution of 4-bromo-2,6-difluoroaniline (5.00 g, 24.0 mmol) and EbN (5.0 mL, 36 mmol) in anhydrous THF (50 mL) was added 4-chlorobutanoyl chloride (3.5 mL, 31 mmol) drop

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, 67567-26-4, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; PETRA PHARMA CORPORATION; LINDSTROeM, Johan; PERSSON, Lars Boukharta; VIKLUND, Jenny; KESICKI, Edward A.; HICKEY, Eugene R.; DAHLGREN, Markus K.; GERASYUTO, Ale

61326-44-1, 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. 61326-44-1, name is 1,1,2,2-Tetrakis(4-bromophenyl)ethene, A new synthetic method of this compound is introduced below.

The 1- (4- (4- (1H-1,2,4-triazol-1-yl) phenoxy) phenyl) -1H-1,2,4-triazoleThe preparation method,Its characteristics in the use of “one pot”In DMF polar solvents,1,1,2,2-tetrakis (4-bromophenyl) ethylene, triazole,The molar ratio of 4,4′-dibromodiphenyl e

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.

Reference:
Patent; Tianjin Normal University; Wang, Ying; (11 pag.)CN104557985; (2017); B;,
Bromide – Wikipedia,

As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 142808-15-9 name is 4-Bromo-2-fluorobenzotrifluoride, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below. 142808-15-9

Preparatory Example27 (3-Fluoro-4- (trifluoromethyl) phenyl) (1-methylcyclopropyl) methanone (Scheme 7): To a solution of 4-bromo-2-fluoro-1- (trifluoromethyl) benzene (0.34 g, 1.4 mmol) in THF (5 mL) at -78under N2was added a solution of isopropylmagnesi

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

Reference:
Patent; MERCK SHARP & DOHME CORP.; MSD R&D (CHINA) CO. LTD.; SHEN, Dong-Ming; DWYER, Michael; SINZ, Christopher J.; WANG, Deping; STACHEL, Shawn; PAONE, Daniel;

937046-98-5, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 937046-98-5 as follows.

Intermediate Rl-A: 7-Bromo-5-iodopyrrolo[2,l-f][l,2,4]triazin-4-amine (Rl-A) To a solution of 7-bromopyrrolo[2,l-f][l,2,4]triazin-4-amine (4 g, 18.78 mmol) in anhydrous DMF (200 mL) was added NIS (4.65 g, 20.65 mmol) and the mixture was stirred in the dar

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 937046-98-5, and friends who are interested can also refer to it.

Reference:
Patent; BRISTOL-MYERS SQUIBB COMPANY; BHIDE, Rajeev S.; RUAN, Zheming; CHERNEY, Robert J.; CORNELIUS, Lyndon A.M.; DHAR, T.G. Murali; GONG, Hua; MARCOUX, David; POSS, M

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 40161-54-4, name is 1-Bromo-2-fluoro-4-(trifluoromethyl)benzene, This compound has unique chemical properties. The synthetic route is as follows., 40161-54-4

Step D 8-(2-Fluoro-4-trifluoromethyl-phenyl)-2-(4-trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one A sealed tube was charged with 4-bromo-3-fluorobenzotrifluoride (40 mg, 0.16 mmol), 2-(4-trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one (5

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.

Reference:
Patent; Ackermann, Jean; Conte, Aurelia; Hunziker, Daniel; Neidhart, Werner; Nettekoven, Matthias; Schulz-Gasch, Tanja; Wertheimer, Stanley; US2012/41013; (2012); A1;

Patent; Kwansei Gakuin Educational Foundation; JNC Corporation; HATAKEYAMA, Takuji; KONDO, Yasuhiro; NAKAMOTO, Keiichi; YANAI, Motoki; (190 pag.)US2018/94000; (2018); A1;,
Author tianliPosted on November 25, 2020Categories 28342-75-8, bromides-buliding-blocksTags M.W=200-300

Patent; Shenzhen Tajirui Bio-pharmaceutical Co., Ltd.; Wang Yihan; Li Huanyin; (24 pag.)CN109232538; (2019); A;,
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