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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086046Generated: November 1, 2026

Acetic Anhydride → HCID 14372570, compound

https://huagongshe.com/reaction/1086046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 14372569HCID 14372569—
SolventDichloromethaneHCID 6344—
ProductHCID 14372570HCID 1437257050%

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 30 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 numberUS05011992
Source datasetuspto-grants-1991_04
ORD IDord-ea88771b7c03408090f766aa6d1592bf
Source noteuspto-grants-1991_04