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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1960440생성일: 2026년 10월 26일

Tributylphosphine → ethyl 7-[(2,2-difluoroethyl)(pyridin-2-ylsulfonyl)amino]-5-(2-methoxyethoxy)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1960440

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물2,2-Difluoroethan-1-olHCID 136187—
반응물ethyl 5-(2-methoxyethoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylateHCID 57476206—
용매TolueneHCID 1140—
생성물ethyl 7-[(2,2-difluoroethyl)(pyridin-2-ylsulfonyl)amino]-5-(2-methoxyethoxy)-1H-indole-2-carboxylateHCID 5747624937%

반응 단계

To a mixture of ethyl 5-(2-methoxyethoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylate (500 mg), 2,2-difluoroethanol (0.09 mL), tributylphosphine (0.59 mL) and toluene (30 mL) was added 1,1′-(azodicarbonyl)dipiperidine (600 mg), and the mixture was stirred at room temperature overnight. The insoluble substance was filtered off, and the filtrate was diluted with ethyl acetate and 1N aqueous hydrochloric acid solution. The organic layer was washed with aqueous sodium bicarbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to basic silica gel column chromatography to give the title compound (211 mg, yield 37%) as a colorless amorphous solid from a fraction eluted with ethyl acetate-hexane (1:4, volume ratio).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410087B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-370627d1dafd44d3928a2a6f45e09438
출처 메모uspto-grants-2013_04