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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1781993생성일: 2026년 10월 26일

Indole-3-Acetic Acid → 1H-Indole-3-acetic acid, 1-[(6-chloroimidazo[2,1-b]thiazol-5-yl)sulfonyl]-

https://huagongshe.com/reaction/1781993

반응식

참여 물질

역할이름HCID투입량
반응물Indole-3-Acetic AcidHCID 802—
반응물6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chlorideHCID 2799717—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1H-Indole-3-acetic acid, 1-[(6-chloroimidazo[2,1-b]thiazol-5-yl)sulfonyl]-HCID 11516775—

반응 단계

A stirred solution of 3-indolylacetic acid (175 mg, 1.00 mmol) in THF is cooled to −78° C. under nitrogen and treated portionwise with 2.5 M n-butyllithium in hexanes (0.84 mL, 2.10 mmol) over a 10 min. period. After 1 h at −78° C., the reaction mixture is treated with (6-chloroimidazo[2,1-b][1,3]thiazol-5-yl)sulfonyl chloride (257 mg, 1.00 mmol) in THF, allowed to warm to ambient temperature, stirred for 24 h and concentrated in vacuo. The resultant residue is treated with 1 M aq HCl (˜2 mL) and water (3 mL) and extracted with dichloromethane. The extracts are combined, dried (MgSO4) and concentrated in vacuo. Chromatography of this residue, eluting with ethyl acetate, affords the title compound as a light tan solid, 32 mg, mp 220-222° C. (darkens>200° C.), identified by mass spectral and NMR analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07498327B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-67b6ab2bb49b4b18a905c4f867c281dc
출처 메모uspto-grants-2009_03