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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620275Generated: November 2, 2026

Acetic Anhydride → HCID 14458154, compound

https://huagongshe.com/reaction/620275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 14372569HCID 14372569—
SolventDichloromethaneHCID 6344—
ProductHCID 14458154HCID 1445815454.1%

Reaction Steps

To a solution of 4-amino-2-(2-aminoethoxy)-5-chloro-N-[2-(diethylamino)ethyl]benzamide (780 mg, 2.4 mmoles) (prepared in Example 47) in methylene chloride was added acetic anhydride (245 mg, 2.4 mmoles) and the mixture stirred for 3 minutes. This was concentrated in vacuo and the residue was partitioned between methylene chloride and sodium bicarbonate solution. The organic phase was concentrated and the residue flash-chromatographed on silica using methylene chloride:methanol:ammonia (100:4:0.5) solvent system. The appropriate fractions were combined and concentrated in vacuo. The residue was recrystallized from methylene chloride-ether to give 445 mg of the title compound as a white solid, mp. 143°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820715
Source datasetuspto-grants-1989_04
ORD IDord-0ce46b7085d246f895112d96ac87636f
Source noteuspto-grants-1989_04