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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867999Generated: November 4, 2026

Cesium carbonate → HCID 86612155, compound

https://huagongshe.com/reaction/1867999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1-Piperidinyloxy, 4-amino-2,2,6,6-tetramethyl-HCID 550942—
Reactant4-Fluorobenzenesulfonic acid 2-(cyclopropanecarbonylamino)-benzothiazol-6-yl esterHCID 11523999—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 86612155HCID 8661215514.6%

Reaction Steps

A solution of 4-fluorobenzenesulfonic acid 2-(cyclopropanecarbonylamino)-benzothiazol-6-yl ester (example 7) (0.352 mmol, 138 mg), 4-amino-TEMPO (0.387 mmol, 66 mg) and cesium carbonate (0.352 mmol, 114 mg) in 3.5 ml of dimethylsulfoxide is stirred for 24 hours. 4-Amino-TEMPO is added twice (2 times 66 mg) after 24 and 48 hours. After 48 hours, the reaction is placed at room temperature for 48 hours. The solution is then diluted with water, extracted with ethyl acetate, washed with saturated sodium chloride solution and dried over sodium sulfate, and then evaporated to dryness, to give 258 mg of crude product. This product is purified by flash chromatography on a cartridge of 5 g of silica. The eluents used are, respectively, dichloromethane and then dichloromethane with 1% of 7M 0.01% ammoniacal methanol. 28 mg of 4-(1-oxyl-2,2,6,6-tetramethylpiperidin-4-ylamino)benzenesulfonic acid 2-(cyclopropanecarbonylamino)benzothiazol-6-yl ester are obtained in a yield of 14%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632952B2
Source datasetuspto-grants-2009_12
ORD IDord-be5970782e66436c863d724f06c03243
Source noteuspto-grants-2009_12