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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510148Generated: November 3, 2026

Cyclohexylamine → HCID 178461164, compound

https://huagongshe.com/reaction/1510148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant921599-76-0HCID 145723817—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 178461164HCID 178461164—

Reaction Conditions

Temperature110 °C

Reaction Steps

Benzyl (5R,7S)-1-(3-fluorophenyl)-4-imino-7-methyl-2-oxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate (27.2 g, 0.066 moles) was dissolved in 100 mL toluene, cyclohexylamine (60 mL, 0.523 moles) was added and the mixture was heated to 110° C. over the weekend in a 1 L roundbottom flask fitted with a condenser. The reaction was diluted with CHCl3 and MeOH until soluble and washed with 1 Normal HCl three times to remove excess cyclohexylamine. The organic was dried with MgSO4, filtered and concentrated to give the product which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211904B2
Source datasetuspto-grants-2012_07
ORD IDord-1844af2d362945088ec415d29b3541bf
Source noteuspto-grants-2012_07