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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260484Generated: October 30, 2026

Acetic Anhydride → HCID 22401469, compound

https://huagongshe.com/reaction/260484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 483550HCID 483550—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22401469HCID 22401469—

Reaction Steps

A solution of N-(3-aminobenzyl) 3-phenylsulfonyl-5-chloroindole-2-carboxamide (Examplle 41) (176 mg, 0.4 mmol) in dry tetrahydrofuran (7 mL) containing acetic anhydride (0.05 mL, 0.5 mmol) was stirred at room temperature for 16 hours. The reaction was diluted with water and extracted with ethyl acetate. The organic layer was dried (Na2SO4), filtered through charcoal, and the solvents evaporated. The residue was triturated with methylene chloride and the solid collected by filtration to give the product, mp 249°-250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527819
Source datasetuspto-grants-1996_06
ORD IDord-453cf328b21945fd85e996151740ad71
Source noteuspto-grants-1996_06