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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52102Generated: October 25, 2026

5-Chlorovaleryl chloride → N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-5-chloropentanamide

https://huagongshe.com/reaction/52102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chlorovaleryl chlorideHCID 74089—
Reactant2-Buten-1-amine, 4-[[4-(1-piperidinylmethyl)-2-pyridinyl]oxy]-, (Z)-HCID 13672473—
ProductN-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-5-chloropentanamideHCID 6772590793%

Reaction Steps

Following a procedure similar to that described in Example 67(a), but using 4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenylamine and 5-chlorovaleryl chloride as starting materials, in relative proportions similar to those used in that Example, the title compound was obtained as an oil in a 93% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616579
Source datasetuspto-grants-1997_04
ORD IDord-304f722ccc9a419a99f92f803e252f20
Source noteuspto-grants-1997_04