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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477661Generated: October 29, 2026

Ammonia → HCID 13588037, compound

https://huagongshe.com/reaction/477661

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 numberUS04888426
Source datasetuspto-grants-1989_12
ORD IDord-527517f28c6f4c668cd9d5c1fb1268bb
Source noteuspto-grants-1989_12