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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818434Generated: October 25, 2026

Cyclohexanone → HCID 57883652, compound

https://huagongshe.com/reaction/1818434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
Reactant2-Amino-5-chlorothiazoleHCID 38942—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 13040867HCID 13040867—
ProductHCID 57883652HCID 57883652—
ProductCyclohex-3-enyl-cyclohexylamineHCID 65702898—

Reaction Steps

Cyclohex-3-enyl-cyclohexylamine was prepared by reductive amination of cyclohex-3-enylamine and cyclohexanone using general procedure (B). Reaction with CDI and 5-chloro-2-aminothiazole using general procedure (A) gave the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598391B2
Source datasetuspto-grants-2009_10
ORD IDord-4645e0cf3d8b47a2a911ca4019b0a3a4
Source noteuspto-grants-2009_10