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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154745Generated: October 25, 2026

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

https://huagongshe.com/reaction/1154745

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 numberUS04490530
Source datasetuspto-grants-1984_12
ORD IDord-7e6f83a538334e12bc722ad209304624
Source noteuspto-grants-1984_12