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HRID 38095作成日:2026年10月26日

Ammonium Chloride → 6-(3-Amino-phenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/38095

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Sodium BicarbonateHCID 516892—
反応物6-(3-Nitrophenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl esterHCID 67424481—
触媒ZincHCID 23994—
溶媒WaterHCID 962—
溶媒1,4-Dioxane--water (1/1)HCID 21886435—
生成物6-(3-Amino-phenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl esterHCID 6742313344.3%

反応条件

温度100 °C

反応手順

6-(3-Nitrophenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl ester (200 mg, 0.508 mmol) was dissolved in a 5:1 dioxane/water mixture (3 mL). Zinc powder (133 mg, 2.03 mmol, 4 eq) and ammonium chloride (271 mg, 5.08 mmol, 10 eq) were added and the mixture was stirred at 100° C. After 4 hours an addition of Zinc powder was made (37 mg) and heating was continued for 1.5 more hours. It was then diluted with water, made basic by addition of saturated aqueous NaHCO3 and extracted with ethyl acetate (3×20 mL). Combined organic layers were washed with sat. aq. NaHCO3 and brine, dried over Na2SO4 and concentrated under reduced pressure. 82 mg of 6-(3-amino-phenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl ester were obtained as off-white solid, which was used without purification in the following step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524707B2
出典データセットuspto-grants-2013_09
ORD IDord-5888b298a98f40cc849fe7fe446253fb
出典メモuspto-grants-2013_09