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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437675Generated: October 30, 2026

Methanol → HCID 68119151, compound

https://huagongshe.com/reaction/437675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 21428804HCID 21428804—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68119151HCID 68119151—

Reaction Steps

A mixture of 4.5 parts of N-{2-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]ethyl}-2-nitrobenzamide, 80 parts of methanol and 45 parts of tetrahydrofuran is hydrogenated at normal pressure and at room temperature with 2 parts of Raney-nickel catalyst. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is crystallized twice from 2-propanol. The product is filtered off and dried, yielding 2 parts of 2-amino-N-{2-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]ethyl}benzamide hemihydrate; mp. 219.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-a3f818f5897b4cf49a0ff0bd917040df
Source noteuspto-grants-1977_06