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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360839생성일: 2026년 10월 24일

Water → 2-chloro-N-[6-(2-chloro-2-phenylacetyl)-6H-pyrazolo[4',3':3,4]benzo[1,2-d]thiazol-2-yl]-2-phenylacetamide

https://huagongshe.com/ko/reaction/1360839

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Chloro(phenyl)acetyl chlorideHCID 102902—
반응물6H-thiazolo[5,4-e]indazol-2-amineHCID 45077674—
용매TetrahydrofuranHCID 8028—
생성물2-chloro-N-[6-(2-chloro-2-phenylacetyl)-6H-pyrazolo[4',3':3,4]benzo[1,2-d]thiazol-2-yl]-2-phenylacetamideHCID 57951435100%

반응 단계

0.50 g (2.6 mmol) of 6H-pyrazolo[4′,3′:3,4]benzo[1,2-d]thiazol-2-ylamine and 1.5 g (7.9 mmol) of α-chlorophenylacetyl chloride were dissolved in 10 ml of tetrahydrofuran, and 1.3 g (12.9 mmol) of triethylamine was added dropwise to the mixture under ice-cooling. After the mixture was allowed to warm to room temperature and was stirred overnight, 10 ml of water was added to the mixture to quench the reaction. The reaction mixture was extracted with 20 ml of ethyl acetate twice, dried over 5 g of anhydrous magnesium sulfate, and then concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (hexane/ethyl acetate=1/1) to give 1.3 g (yield: 100%) of 2-chloro-N-[6-(2-chloro-2-phenylacetyl)-6H-pyrazolo[4′,3′:3,4]benzo[1,2-d]thiazol-2-yl]-2-phenylacetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879887B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-bccc2275fb4d4150b45000767e7823ce
출처 메모uspto-grants-2011_02