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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1949169생성일: 2026년 10월 27일

Hexane → 2-[2-(phenylsulfonyl)ethylthio]-N-(2-thienyl-methyl)-3-quinoline carboxamide

https://huagongshe.com/reaction/1949169

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참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물2-(Phenylsulfonyl)ethanethiolHCID 447093—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamideHCID 86645338—
용매DimethylformamideHCID 6228—
생성물2-[2-(phenylsulfonyl)ethylthio]-N-(2-thienyl-methyl)-3-quinoline carboxamideHCID 4691159270%

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온도0 °C

반응 단계

112 mg (1.0 mmol) potassium tert-butylate were added to a solution of 202 mg (1.0 mmol) 2-(phenylsulfonyl)ethanethiol in DMF (6 ml) at 0° C. and the mixture was stirred for 10 min at 0° C. Then 303 mg (1.0 mmol) 2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamide (precursor VVV01) were added at 0° C. and the reaction solution was heated slowly to 50° C. and stirred for 16 h at this temperature. After cooling to RT it was diluted with EE and washed with a saturated aqueous NH4Cl solution. The aqueous phase was extracted with EE. The combined organic phases were washed with water and brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 4:1) with the residue yielded 326 mg (0.7 mmol, 70%) 2-[2-(phenylsulfonyl)ethylthio]-N-(2-thienyl-methyl)-3-quinoline carboxamide. MS: m/z 469.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399673B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-048edb2dfbb94e89942963be76ab4fdb
출처 메모uspto-grants-2013_03