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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38073생성일: 2026년 10월 25일

Ammonium Chloride → 3-(7-Pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine

https://huagongshe.com/reaction/38073

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1,4-Dioxane--water (1/1)HCID 21886435—
반응물6-(3-Nitro-phenyl)-7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazoleHCID 67423036—
촉매ZincHCID 23994—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물3-(7-Pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenylamineHCID 4692918373.4%

반응 조건

온도100 °C

반응 단계

6-(3-Nitro-phenyl)-7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazole (150 mg, 0.463 mmol) was suspended in a 5:1 dioxane/water mixture (3 mL). Zinc powder (121 mg, 1.852 mmol, 4 eq) was added, followed by ammonium chloride (247 mg, 4.63 mmol, 10 eq) and the mixture was heated to 100° C. and stirred at the same temperature for 2 hours. The reaction mixture was then allowed to cool to room temperature and diluted with water and ethyl acetate. The aqueous phase was basified by adding solid Na2HPO4 and extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with saturated aqueous NaHCO3 and brine, dried and concentrated to dryness. 100 mg of 3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine were obtained as off-white solid (73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524707B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-466421725f78485f95cc449635479323
출처 메모uspto-grants-2013_09