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HRID 1793857생성일: 2026년 10월 25일

3-(2-Bromoethyl)indole → 3-(2-Bromoethyl)-1-(6-chloroimidazo[2,1-b]thiazole-5-sulfonyl)indole

https://huagongshe.com/reaction/1793857

반응식

참여 물질

역할이름HCID투입량
반응물3-(2-Bromoethyl)indoleHCID 76924—
반응물6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chlorideHCID 2799717—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물3-(2-Bromoethyl)-1-(6-chloroimidazo[2,1-b]thiazole-5-sulfonyl)indoleHCID 1125934958%

반응 단계

A mixture of 3-(2-bromoethyl)indole (1.0 g, 4.46 mmol) and 6-chloroimidazo[2,1-b]thiazole-5-sulfonyl chloride (0.96 g, 1.1 eq.) in THF is treated with potassium t-butoxide (0.48 g, 1.1 equiv.) at room temperature, stirred for 16 h, quenched with saturated NaHCO3 and extracted with EtOAc. The extracts are combined, dried over MgSO4 and concentrated in vacuo to give the title product as a brown oil, 1.2 g (58% yield), identified by HPLC and mass spectral analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07022701B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-6727cf8fca674d6b87d64708b6652158
출처 메모uspto-grants-2006_04