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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886415Generated: November 2, 2026

Ammonia → HCID 15037481, compound

https://huagongshe.com/reaction/1886415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 15037525HCID 15037525—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 15037481HCID 1503748191%

Reaction Steps

A mixture of 11 parts of 3-[[1-(2-pyridinylmethyl)-1H-benzimidazol-2-yl]amino]-1-pyrrolidineacetonitrile and 320 parts of methanol, saturated with ammonia was hydrogenated at normal pressure and at room temperature with 3 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 solidified in 2,2'-oxybispropane while stirring. The product was filtered off and dried, yielding 10 parts (91%) of N-[1-(2-aminoethyl)-3-pyrrolidinyl]-1-(2-pyridinylmethyl)-1H-benzimidazol-2-amine; mp. 130° C. (compound 138).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151424
Source datasetuspto-grants-1992_09
ORD IDord-c6aa1ad5c5934e03880423d2105e6e8c
Source noteuspto-grants-1992_09