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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1781993Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1781993

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndole-3-Acetic AcidHCID 802—
Edukt6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chlorideHCID 2799717—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1H-Indole-3-acetic acid, 1-[(6-chloroimidazo[2,1-b]thiazol-5-yl)sulfonyl]-HCID 11516775—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07498327B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-67b6ab2bb49b4b18a905c4f867c281dc
Quellennotizuspto-grants-2009_03