Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493910Generated: October 31, 2026

Ammonia → HCID 13588037, compound

https://huagongshe.com/reaction/1493910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantHCID 13588013HCID 13588013—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
ProductHCID 13588037HCID 1358803778%

Reaction Steps

A mixture of 12 parts of 4-[[1-[(4-fluorophenyl)methyl]-1H-imidazo[4,5-b]pyridin-2-yl]amino]-1-piperidineacetonitrile and 200 parts of methanol saturated with ammonia was hydrogenated at normal pressure and at room temperature 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 crystallized from acetonitrile, yielding 10 parts (78%) of N-[1-(2-aminoethyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-imidazo[4,5-b]pyridin-2-amine monohydrate; mp. 116.9° C. (intermediate 109).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025014
Source datasetuspto-grants-1991_06
ORD IDord-400a2e3cdf3542a5bf950ee35039081c
Source noteuspto-grants-1991_06