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HRID 1949169作成日:2026年10月27日

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

https://huagongshe.com/reaction/1949169

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物2-(Phenylsulfonyl)ethanethiolHCID 447093—
反応物Potassium tert-butoxideHCID 23665647—
反応物2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamideHCID 86645338—
溶媒DimethylformamideHCID 6228—
生成物2-[2-(phenylsulfonyl)ethylthio]-N-(2-thienyl-methyl)-3-quinoline carboxamideHCID 4691159270%

反応条件

温度0 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08399673B2
出典データセットuspto-grants-2013_03
ORD IDord-048edb2dfbb94e89942963be76ab4fdb
出典メモuspto-grants-2013_03