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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38095생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Sodium BicarbonateHCID 516892—
반응물6-(3-Nitrophenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl esterHCID 67424481—
촉매ZincHCID 23994—
용매WaterHCID 962—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물6-(3-Amino-phenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl esterHCID 6742313344.3%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524707B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5888b298a98f40cc849fe7fe446253fb
출처 메모uspto-grants-2013_09