戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1781993作成日:2026年10月27日

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

https://huagongshe.com/reaction/1781993

反応式

関与物質

役割名称HCID仕込み量
反応物Indole-3-Acetic AcidHCID 802—
反応物6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chlorideHCID 2799717—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1H-Indole-3-acetic acid, 1-[(6-chloroimidazo[2,1-b]thiazol-5-yl)sulfonyl]-HCID 11516775—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07498327B2
出典データセットuspto-grants-2009_03
ORD IDord-67b6ab2bb49b4b18a905c4f867c281dc
出典メモuspto-grants-2009_03