Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164235Generated: October 26, 2026

Pyridine → Phenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamate

https://huagongshe.com/reaction/1164235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiisopropyl EtherHCID 7914—
ReactantPhenyl chloroformateHCID 15891—
ReactantBenzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-HCID 154406—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductPhenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamateHCID 98160761%

Reaction Steps

A mixture of 6 parts of 4-[4-(4-methoxyphenyl)-1-piperazinyl]benzenamine, 3.6 parts of phenyl carbonochloridate, 75 parts of pyridine and 98 parts of dichloromethane is stirred and warmed till all solid enters solution. Stirring is continued for 30 minutes at room temperature. The reaction mixture is poured onto 500 parts of water and 210 parts of 2,2'-oxybispropane are added. The whole is stirred for a while. The precipitated product is filtered off and crystallized from 1-butanol, yielding 5.2 parts (61%) of phenyl{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}carbamate; mp. 204.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04368200
Source datasetuspto-grants-1983_01
ORD IDord-c728eed3e3784f39854ff3fd7bdb9062
Source noteuspto-grants-1983_01