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HRID 1423041作成日:2026年10月25日

tert-Butylsulfinamide, (R)-(+)- → (NZ)-2-methyl-N-[1-(2-methylsulfonyl-1,3-thiazol-5-yl)propylidene]propane-2-sulfinamide

https://huagongshe.com/reaction/1423041

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
反応物1-(2-Methanesulfonyl-thiazol-5-yl)-propan-1-oneHCID 59278397—
触媒Titanium isopropoxideHCID 11026—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物(NZ)-2-methyl-N-[1-(2-methylsulfonyl-1,3-thiazol-5-yl)propylidene]propane-2-sulfinamideHCID 87126692—

反応手順

A mixture of 1-(2-methanesulfonyl-thiazol-5-yl)-propan-1-one (110 mg, 0.50 mmol), (R)-2-methyl-2-propanesulfinamide (70 mg, 0.6 mmol) and titanium (IV) isopropoxide (0.29 mL, 1.0 mmol) in THF (10 mL) is warmed at reflux. After 18 hours, the mixture is cooled to room temperature and diluted with diethyl ether (100 mL) and water (6 mL). After 10 minutes with stirring, the solution is dried over sodium sulfate, filtered and concentrated. The crude product is purified by silica gel chromatography eluting with a gradient of 0-100% EtOAc in hexanes to afford 2-methyl-propane-2-sulfinic acid [1-(2-methanesulfonyl-thiazol-5-yl)-prop-(Z)-ylidene]-amide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08927550B2
出典データセットuspto-grants-2015_01
ORD IDord-cd07506f52b145dbb3b0cede6d322b09
出典メモuspto-grants-2015_01