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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867990Generated: November 1, 2026

Water → 4-(2-Isopropylaminoethylamino)benzenesulfonic acid 2-(cyclopentanecarbonyl-amino)benzothiazol-6-yl ester

https://huagongshe.com/reaction/1867990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
ReactantN-IsopropylethylenediamineHCID 88098—
Reactant4-Fluorobenzenesulfonic acid 2-(2-methoxy-acetylamino)benzothiazol-6-yl esterHCID 57980854—
SolventDimethyl SulfoxideHCID 679—
Product4-(2-Isopropylaminoethylamino)benzenesulfonic acid 2-(cyclopentanecarbonyl-amino)benzothiazol-6-yl esterHCID 5798083948.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 4-fluorobenzenesulfonic acid 2-(2-methoxyacetylamino)-benzothiazol-6-yl ester (intermediate 68) (90 mg, 0.214 mmol), N-isopropylethylenediamine (65.6 mg, 0.642 mmol) and cesium carbonate (69.7 mg, 0.214 mmol) in 2 ml of dimethyl sulfoxide in a test tube, equipped with a magnetic bar, is stirred overnight at 80° C. 100 ml of water are added and the reaction medium is extracted with ethyl acetate. The organic phase is then washed with water, dried over magnesium sulfate and evaporated. The residue, purified by LC/MS, gives 26.2 mg of 4-(2-isopropylaminoethylamino)benzenesulfonic acid 2-(cyclopentanecarbonyl-amino)benzothiazol-6-yl ester (white powder) in a yield of 24%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632952B2
Source datasetuspto-grants-2009_12
ORD IDord-5b5b3b01394f45129a079e55ce8a809f
Source noteuspto-grants-2009_12