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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867964Generated: October 30, 2026

4-(4-(Pyridin-3-yl)-1H-imidazol-1-yl)butan-1-amine → 4-[4-(4-Pyrid-3-ylimidazol-1-yl)butylamino]-benzenesulfonic 2-(cyclopropanecarbonylamino)benzothiazol-6-yl ester

https://huagongshe.com/reaction/1867964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-(Pyridin-3-yl)-1H-imidazol-1-yl)butan-1-amineHCID 11042160—
Reactant4-Fluorobenzenesulfonic acid 2-(cyclopropanecarbonylamino)-benzothiazol-6-yl esterHCID 11523999—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-[4-(4-Pyrid-3-ylimidazol-1-yl)butylamino]-benzenesulfonic 2-(cyclopropanecarbonylamino)benzothiazol-6-yl esterHCID 11541608—

Reaction Steps

A solution of 4-fluorobenzenesulfonic 2-(cyclopropanecarbonylamino)benzo-thiazol-6-yl ester (example 7) (50 mg, 127.4 μmol) and 4-(4-pyrid-3-ylimidazol-1-yl)butylamine (110.2 mg, 0.51 mmol) in 0.5 ml of NMP is heated at 150° C. by microwave for 8 minutes. The crude reaction product is purified by preparative LC/MS (basic medium (pH 9)) to give after freeze-drying 36 mg of 4-(2-hydroxy-2-methylpropylamino)benzenesulfonic 2-(cyclo-propanecarbonylamino)benzothiazol-6-yl ester (beige-colored solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632952B2
Source datasetuspto-grants-2009_12
ORD IDord-addae98b79d54e2e9731d9f40046de6f
Source noteuspto-grants-2009_12