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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Indole-3-Acetic Acid | HCID 802 | — |
| 반응물 | 6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chloride | HCID 2799717 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1H-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07498327B2 |
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| 출처 데이터셋 | uspto-grants-2009_03 |
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| ORD ID | ord-67b6ab2bb49b4b18a905c4f867c281dc |
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| 출처 메모 | uspto-grants-2009_03 |
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