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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1480250생성일: 2026년 10월 27일

Heptane → N-[2-cyclopropyl-1-methyl-1-(5-methylthiazol-2-yl)ethyl]-2-methyl-propane-2-sulfinamide

https://huagongshe.com/reaction/1480250

반응식

참여 물질

역할이름HCID투입량
반응물HeptaneHCID 8900—
반응물5-MethylthiazoleHCID 137980—
반응물Lithium diisopropylamideHCID 2724682—
반응물TrimethylaluminumHCID 16682925—
반응물(NE)-N-(1-cyclopropylpropan-2-ylidene)-2-methylpropane-2-sulfinamideHCID 89424933—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물N-[2-cyclopropyl-1-methyl-1-(5-methylthiazol-2-yl)ethyl]-2-methyl-propane-2-sulfinamideHCID 9020413055%

반응 조건

온도-78 °C

반응 단계

A 2.0M solution of lithium diisopropylamide in THF (745 μl, 1.49 mmol) was added dropwise to a solution of 5-methylthiazole (148 mg, 1.49 mmol) in dry THF (0.5 ml) cooled to −78° C. and once the addition was complete the reaction was stirred for 30 minutes at −78° C. followed by addition of dry toluene (1.5 ml). To a solution of (NE)-N-(2-cyclopropyl-1-methyl-ethylidene)-2-methyl-propane-2-sulfinamide (CAN 1426426-70-1, 150 mg, 745 μmol) in dry toluene (1.5 mL) was added a 2.0M solution of trimethylaluminum in heptane (410 μl, 820 μmol). The previous solution was then added to the reaction mixture cooled at −78° C. The reaction was allowed to warm up to room temperature overnight. The reaction was quenched by the addition of a saturated aqueous solution of ammonium chloride and was then diluted with ethyl acetate. The bi-phasic mixture was poured into a separatory funnel and extracted. The organic phase was collected, dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a heptane/ethyl acetate gradient to yield the title compound (123 mg, 55%). MS (ESI, m/z): 301.4 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409866B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-1e2c2ff3bbc14a9e8fe1d5f2c5b24baf
출처 메모uspto-grants-2016_08