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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68813Generated: October 28, 2026

N-(1-Cyano-piperidin-4-yl)-N-cyclopropyl-4-oxazol-5-yl-benzamide → N-[1-(3-Allyl-[1,2,4]oxadiazol-5-yl)-piperidin-4-yl]-N-cyclopropyl-4-oxazol-5-yl-benzamide

https://huagongshe.com/reaction/68813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-Cyano-piperidin-4-yl)-N-cyclopropyl-4-oxazol-5-yl-benzamideHCID 86678209—
ReactantHCID 178449907HCID 178449907—
ProductN-[1-(3-Allyl-[1,2,4]oxadiazol-5-yl)-piperidin-4-yl]-N-cyclopropyl-4-oxazol-5-yl-benzamideHCID 68351843—

Reaction Steps

The title compound is prepared from N-(1-cyano-piperidin-4-yl)-N-cyclopropyl-4-oxazol-5-yl-benzamide and N-hydroxy-but-3-enamidine following a procedure analogous to that described in Example 1. LC (method 6): tR=1.65 min; Mass spectrum (ESI+): m/z=420 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822471B2
Source datasetuspto-grants-2014_09
ORD IDord-9f54a4b55281452287c0a6b49703e7b7
Source noteuspto-grants-2014_09