Category: 79456-33-0

Related Products of 79456-33-0, 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.79456-33-0, name is 5-Chloro-3-(trifluoromethyl)pyridin-2-amine, molecular formula is C6H4ClF3N2, molecular weight is 196.56, as common compound, the synthetic route is as follows.

To a stirred solution of 5-chloro-3-(trifluoromethyl)pyridin-2-amine (Intermediate 47; CAS79456-33-0, 10 g, 50.9 mmol) in aqueous HBr (48 %, 56.7 g, 336 mmol) at -10 C wasadded bromine (23.6 g, 147.5 mmol) dropwise over 20 minutes, followed by a solution ofsodium nitrite (10.2 g, 147.8 mmol) in water (18 mL). The reaction was stirred at ambienttemperature for 2 hours and was basified (pH 9-10) and extracted into diethyl ether. Theorganic was washed with brine, dried (Na2504), filtered and concentrated in vacuo toafford the title compound without further purification.MS ES: 262

The chemical industry reduces the impact on the environment during synthesis 79456-33-0, I believe this compound will play a more active role in future production and life.

Reference:
Patent; TAKEDA CAMBRIDGE LIMITED; TAKEDA PHARMACEUTICAL COMPANY LIMITED; GOLDBY, Anne; JENKINS, Kerry; TEALL, Martin; WO2015/79224; (2015); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Related Products of 79456-33-0, 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.79456-33-0, name is 5-Chloro-3-(trifluoromethyl)pyridin-2-amine, molecular formula is C6H4ClF3N2, molecular weight is 196.56, as common compound, the synthetic route is as follows.

To a stirred solution of 5-chloro-3-(trifluoromethyl)pyridin-2-amine (Intermediate 47; CAS79456-33-0, 10 g, 50.9 mmol) in aqueous HBr (48 %, 56.7 g, 336 mmol) at -10 C wasadded bromine (23.6 g, 147.5 mmol) dropwise over 20 minutes, followed by a solution ofsodium nitrite (10.2 g, 147.8 mmol) in water (18 mL). The reaction was stirred at ambienttemperature for 2 hours and was basified (pH 9-10) and extracted into diethyl ether. Theorganic was washed with brine, dried (Na2504), filtered and concentrated in vacuo toafford the title compound without further purification.MS ES: 262

The chemical industry reduces the impact on the environment during synthesis 79456-33-0, I believe this compound will play a more active role in future production and life.

Reference:
Patent; TAKEDA CAMBRIDGE LIMITED; TAKEDA PHARMACEUTICAL COMPANY LIMITED; GOLDBY, Anne; JENKINS, Kerry; TEALL, Martin; WO2015/79224; (2015); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Related Products of 79456-33-0, 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.79456-33-0, name is 5-Chloro-3-(trifluoromethyl)pyridin-2-amine, molecular formula is C6H4ClF3N2, molecular weight is 196.56, as common compound, the synthetic route is as follows.

To a stirred solution of 5-chloro-3-(trifluoromethyl)pyridin-2-amine (Intermediate 47; CAS79456-33-0, 10 g, 50.9 mmol) in aqueous HBr (48 %, 56.7 g, 336 mmol) at -10 C wasadded bromine (23.6 g, 147.5 mmol) dropwise over 20 minutes, followed by a solution ofsodium nitrite (10.2 g, 147.8 mmol) in water (18 mL). The reaction was stirred at ambienttemperature for 2 hours and was basified (pH 9-10) and extracted into diethyl ether. Theorganic was washed with brine, dried (Na2504), filtered and concentrated in vacuo toafford the title compound without further purification.MS ES: 262

The chemical industry reduces the impact on the environment during synthesis 79456-33-0, I believe this compound will play a more active role in future production and life.

Reference:
Patent; TAKEDA CAMBRIDGE LIMITED; TAKEDA PHARMACEUTICAL COMPANY LIMITED; GOLDBY, Anne; JENKINS, Kerry; TEALL, Martin; WO2015/79224; (2015); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Reference of 79456-33-0, 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. 79456-33-0, name is 5-Chloro-3-(trifluoromethyl)pyridin-2-amine, molecular formula is C6H4ClF3N2, The 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.

Step B ethyl 6-chloro-8-(trifluoromethyl)imidazo[l,2-a]pyridine-2-carboxylate[0121] 5-chloro-3-(trifluoromethyl)-2-pyridinamine (3.0 g, 15 mmol) and ethyl bromopyruvate (4.27 mL, 30.5 mmol) in N,N-dimethylformamide (50 mL) were stirred at 60 0C for 3 hours. The mixture was allowed to cool and then poured into stirring iced water. The precipitate was stirred for 5 minutes, collected by filtration, washed with water, and dried under vacuum to give the title compound (3.5 g; 78%). LCMS: m/z 293, 295 (M+l).

According to the analysis of related databases, 79456-33-0, the application of this compound in the production field has become more and more popular.

Reference:
Patent; GLAXOSMITHKLINE LLC; BANKA, Anna; BASKARAN, Subramanian; CATALANO, John; CHONG, Pek; DICKSON, Hamilton; FANG, Jing; MAUNG, Jack; NEITZEL, Martin, Leon; PEAT, Andy; PRICE, Daniel; RAI, Roopa; ROBERTS, Christopher, Don; SHOTWELL, Brad; TAI, Vincent; ZHANG, Huichang; WO2010/91411; (2010); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Reference of 79456-33-0, 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. 79456-33-0, name is 5-Chloro-3-(trifluoromethyl)pyridin-2-amine, molecular formula is C6H4ClF3N2, The 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.

Step B ethyl 6-chloro-8-(trifluoromethyl)imidazo[l,2-a]pyridine-2-carboxylate[0121] 5-chloro-3-(trifluoromethyl)-2-pyridinamine (3.0 g, 15 mmol) and ethyl bromopyruvate (4.27 mL, 30.5 mmol) in N,N-dimethylformamide (50 mL) were stirred at 60 0C for 3 hours. The mixture was allowed to cool and then poured into stirring iced water. The precipitate was stirred for 5 minutes, collected by filtration, washed with water, and dried under vacuum to give the title compound (3.5 g; 78%). LCMS: m/z 293, 295 (M+l).

According to the analysis of related databases, 79456-33-0, the application of this compound in the production field has become more and more popular.

Reference:
Patent; GLAXOSMITHKLINE LLC; BANKA, Anna; BASKARAN, Subramanian; CATALANO, John; CHONG, Pek; DICKSON, Hamilton; FANG, Jing; MAUNG, Jack; NEITZEL, Martin, Leon; PEAT, Andy; PRICE, Daniel; RAI, Roopa; ROBERTS, Christopher, Don; SHOTWELL, Brad; TAI, Vincent; ZHANG, Huichang; WO2010/91411; (2010); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem