Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225361Generated: October 25, 2026

Amoxapine → Ethyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinecarboxylic Acid Ester

https://huagongshe.com/reaction/2225361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmoxapineHCID 2170—
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinecarboxylic Acid EsterHCID 1900407497%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2.20 g of 2-chloro-11-(1-piperazinyl)dibenz[b,f][1,4]oxazepine, 0.76 g of ethyl chloroformate and 0.97 g of potassium carbonate in 20 ml of N,N-dimethylformamide was stirred at 80° C. for 3 hrs. Ice water was added to the reaction mixture and extracted with ether. The etheral layer was washed with water, dried and concentrated. The residue was chromatographed on silica gel using a mixture of n-hexane and ethyl acetate (1:2) as eluents to give 2.62 g of colorless crystals, which were recrystallized from isopropyl ether to give colorless prisms, mp 121.5°-122.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344828
Source datasetuspto-grants-1994_09
ORD IDord-3a7d3ae34f4c4c6cb85cf3f4240a1400
Source noteuspto-grants-1994_09