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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1361188생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1361188

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) was warmed at reflux for 18 hours. The mixture was cooled to room temperature and diluted with diethyl ether (100 mL) and water (6 mL). After 10 minutes with stirring, the solution was dried over sodium sulfate, filtered and concentrated. The crude product was 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 번호US07879873B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-cfa7a60ab298436d9e2b4c03a749b674
출처 메모uspto-grants-2011_02