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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52085Generated: October 25, 2026

N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-chlorobutyramide → N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-(1-methyltetrazol-5-ylthio)butyramide

https://huagongshe.com/reaction/52085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-chlorobutyramideHCID 67726214—
ReactantHCID 178482017HCID 178482017—
ProductN-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-(1-methyltetrazol-5-ylthio)butyramideHCID 6772596670%

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 1-methyl-5-mercaptotetrazole as starting materials, in relative proportions similar to those used in that Example, the title compound was obtained as an oil in a 70% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616579
Source datasetuspto-grants-1997_04
ORD IDord-51a1c8ca794a44c4b38fe0ea28843ee5
Source noteuspto-grants-1997_04