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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1423041생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1423041

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
반응물1-(2-Methanesulfonyl-thiazol-5-yl)-propan-1-oneHCID 59278397—
촉매Titanium isopropoxideHCID 11026—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물(NZ)-2-methyl-N-[1-(2-methylsulfonyl-1,3-thiazol-5-yl)propylidene]propane-2-sulfinamideHCID 87126692—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08927550B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-cd07506f52b145dbb3b0cede6d322b09
출처 메모uspto-grants-2015_01