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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262734Generated: November 3, 2026

Acetic Anhydride → HCID 11983398, compound

https://huagongshe.com/reaction/2262734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 11983378HCID 11983378—
SolventDichloromethaneHCID 6344—
ProductHCID 11983398HCID 1198339865%

Reaction Steps

To a suspension of C-[1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-yl]-methylamine (0.70 g, 2.3 mmol) in dichloromethane (30 ml) was added acetic anhydride (2.4 ml, 2.5 mmol) dropwise with stirring. After the addition, stirring was continued for 30 min and the reaction mixture was washed twice with saturated, aqueous sodium bicarbonate and once with water. The organic phase was dried over sodium sulfate and concentrated in vacuo. The concentrate was purified by column chromatography on silica gel, eluting with a mixture of dichloromethane, methanol and ammonia (9:1:0.1 v/v/v). This afforded the desired product (0.52 g, 65%). Mp. 156.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851490B2
Source datasetuspto-grants-2010_12
ORD IDord-d7b3db336e1b4f63b5ebf1aceb1ab988
Source noteuspto-grants-2010_12