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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1697256생성일: 2026년 10월 26일

2-Bromothiazole → HCID 67269896, 화합물

https://huagongshe.com/reaction/1697256

반응식

참여 물질

역할이름HCID투입량
반응물2-BromothiazoleHCID 76430—
반응물(NE,S)-N-[(2S)-2,3-bis[[tert-butyl(dimethyl)silyl]oxy]propylidene]-2-methylpropane-2-sulfinamideHCID 44239381—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물HCID 67269896HCID 6726989683%

반응 단계

A solution of 2-bromothiazole (7.9 ml, 89 mmol) in 200 mL ether was cooled to −78° C. and treated with a solution of n-butyllithium (36 ml, 89 mmol) (2.5N in hexanes). After stirring for 30 minutes the reaction mixture was slowly added to a cooled (−78° C.) suspension of (S,E)-N—((S)-2,3-bis(tert-butyldimethylsilyloxy)propylidene)-2-methylpropane-2-sulfinamide (25.000 g, 59 mmol) in 100 mL ether. The reaction mixture was allowed to stir at −78° C. for one hour. The reaction mixture was quenched with MeOH and saturated NH4Cl solution. The organic solution was washed with water, brine, dried over MgSO4 and concentrated in vacuo. Purification of the crude residue by column chromatography gave (S)—N-((1R,2S)-2,3-bis(tert-butyldimethylsilyloxy)-1-(thiazol-2-yl)propyl)-2-methylpropane-2-sulfinamide (24.81 g, 83% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163909B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-94bd15697fa24e409acd93184e48aa52
출처 메모uspto-grants-2012_04