Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980571Generated: October 31, 2026

N-Methylcyclohexylamine → HCID 20401994, compound

https://huagongshe.com/reaction/1980571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13044649HCID 13044649—
SolventChloroformHCID 6212—
ProductHCID 20401994HCID 2040199479%

Reaction Steps

In 50 ml of chloroform was dissolved 4.6 g of 1-(4-chloro-6-quinazolinesulfonyl)-4-(2-ethoxy-2-phenylethyl)piperazine, and to the solution were added 1.7 g of N-methyl-N-cyclohexylamine and 1 g of anhydrous potassium carbonate, and the mixture was stirred at a temperature of 20° C. to 25° C. for 3 hours. The reaction solution thus obtained was washed with water, dried with anhydrous potassium carbonate and then chloroform was distilled therefrom. The residue was subjected to the same silica gel-column chromatography as in Example 1 using chloroform as the solvent for purification to give 4.2 g of 1-[4-(N-methyl-N-cyclohexylamino)-6-quinazolinesulfonyl]-4-(2-ethoxy-2-phenylethyl)piperazine [i.e., Compound (19)] in a yield of 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510307
Source datasetuspto-grants-1985_04
ORD IDord-6d83824fc20e423bb89bc0542e214af1
Source noteuspto-grants-1985_04