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N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine

 структура
444731-74-2
CAS №
444731-74-2
английское имя:
N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine
Синонимы:
BNKY007-PZ01;Pazopanib Impurity 20;2H-indazol-6aMine,2,3-diMethyl.HCl(1:1);N-(2-chloropyrimidin-4-yl)-2,3-dimethylindazol-6-amine;N-(2-chloro-4-pyriMidinyl)-2,3-diMethyl-2H-indazol-6-aMine;N-(2-chloropyriMidin-4-yl)-2,3-diMethyl-2H- indazol-6-aMine;2H-Indazol-6-aMine, N-(2-chloro-4-pyriMidinyl)-2,3-diMethyl-;6-[N-(2-chloropyriMidin-4-yl)aMino]-2,3-diMethyl-2H-indazole;N-(2-chloropyrimidin-4-yl)-N,2,3-dimethyl-2H-indazol -6-amine;N-(2-chloropyriMidin-4-yl)-2,3-diMethyl-2H- indazol-6-aMine ISO 9001:2015 REACH
CBNumber:
CB12526161
Формула:
C13H12ClN5
молекулярный вес:
273.72
MOL File:
444731-74-2.mol

N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine атрибут

Температура плавления: >216oC (dec.)
Температура кипения: 550.0±35.0 °C(Predicted)
плотность: 1.41±0.1 g/cm3(Predicted)
температура хранения: Hygroscopic, Refrigerator, under inert atmosphere
растворимость: Хлороформ (Мало растворим), ДМСО (Мало растворим), метанол (Мало растворим)
форма: Твердый
пка: 2.56±0.30(Predicted)
цвет: От бледно-оранжевого до светло-коричневого
Стабильность:: гигроскопичный

Заявления о рисках и безопасности

N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine химические свойства, назначение, производство

Использование

N-(2-Chloro-4-pyrimidinyl)-2,3-dimethyl-2H-indazol-6-amine (N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine) is an impurity of Pazopanib (P210925), an oral angiogenesis inhibitor targeting VEGFR and PDGFR.

прикладной

N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine is a valuable organic compound that could be used to synthesize N-(2-chloropyrimidin-4-yl)-N,2,3-trimethyl-2H-indazol-6-amine, N- (2-chloropyrimidin-4-yl)-N,2,3-trimethyl-2H-indazol-6-amine, and others.

Синтез

2,3-dimethyl-6-amino-2H- indazole 5.00g,2,4-Dichloropyrimidine 13.9g and sodium bicarbonate 10.4g were dissolved in 100mL absolute ethanol and heated to 79°C.After refluxing for 4 h, cool to room temperature and filter. The cake was washed well with ethyl acetate, and the filtrate was collected. Concentrate under reduced pressure, remove the solvent, and fully beat with ethyl acetate and filter to give an off-white solid. Recrystallization from methanol gave 7.64 g of product N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine as a white solid, yield: 90.0%. N-(2-chloropyriMidin-4-yl)-2,3-diMethyl-2H- indazol-6-aMine

N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine препаратная продукция и сырье

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N-(2-Chloropyrimidin-4-YL)-2,3-dimethyl-2H-indazol-6-amine поставщик

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