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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893672Generated: October 29, 2026

Ammonia → HCID 13588037, compound

https://huagongshe.com/reaction/893672

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 numberUS05126339
Source datasetuspto-grants-1992_06
ORD IDord-5ef0f3acc56f48b888a4a9c63550eade
Source noteuspto-grants-1992_06