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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309501Generated: October 30, 2026

Ammonia → HCID 13588037, compound

https://huagongshe.com/reaction/2309501

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 numberUS04695569
Source datasetuspto-grants-1987_09
ORD IDord-340deba50e3d49f99bd24fa781a7a586
Source noteuspto-grants-1987_09