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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52078Generated: October 26, 2026

N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-chlorobutyramide → N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-(1-methylimidazol-2-ylthio)butyramide

https://huagongshe.com/reaction/52078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-chlorobutyramideHCID 67726214—
ReactantHCID 178480602HCID 178480602—
ProductN-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-(1-methylimidazol-2-ylthio)butyramideHCID 6772608549%

Reaction Steps

Following a procedure similar to that described in Example 34, but using N-[4-(4-piperidinomethyl-2-pyridyloxy) -cis-2-butenyl]-4-chlorobutyramide (prepared as described in Preparation 2) and 2-mercapto-1-methylimidazole as starting materials, in relative proportions similar to those used in that Example, the title compound was obtained as an oil in a 49% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616579
Source datasetuspto-grants-1997_04
ORD IDord-479647c07f324711b5e3fc25c5405b43
Source noteuspto-grants-1997_04