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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165034Generated: October 31, 2026

Ammonia → HCID 14854959, compound

https://huagongshe.com/reaction/1165034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactantcis-4-amino-5-chloro-N-[1-(2-cyanoethyl)-3-methoxy-4-piperidinyl]-2-methoxybenzamideHCID 67915944—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 14854959HCID 1485495913%

Reaction Steps

A mixture of 3 parts of cis-4-amino-5-chloro-N-[1-(2-cyanoethyl)-3-methoxy-4-piperidinyl]-2-methoxybenzamide and 200 parts of methanol, saturated with ammonia was hydrogenated at normal pressure and at 20° C. with 2 parts of Raney-nickel catalyst. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was dissolved in trichloromethane. The solution was washed with water, dried, filtered and evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried in vacuo at 60° C., yielding 0.4 parts (13%) of cis-4-amino-N-[1-(3-aminopropyl)-3-methoxy-4-piperidinyl]-5-chloro-2-methoxybenzamide; mp. 174.8 (interm. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906643
Source datasetuspto-grants-1990_03
ORD IDord-a71cc7813549468a9696bc9593930ee5
Source noteuspto-grants-1990_03