HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345585Generated: October 30, 2026
HCID 15096760, compound → cis-1-(1H-benzimidazol-2-ylmethyl)-3-methoxy-4-piperidinamine dihydrate
https://huagongshe.com/reaction/345585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15096760 | HCID 15096760 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | cis-1-(1H-benzimidazol-2-ylmethyl)-3-methoxy-4-piperidinamine dihydrate | HCID 67946490 | — |
Reaction Steps
A mixture of 18 parts of cis-1-(1H-benzimidazol-2ylmethyl)-3-methoxy-N-(phenylmethyl)-4-piperidinamine and 200 parts of methanol was hydrogenated at normal pressure and at room temperature with 3 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (93:7 by volume), saturated with ammonia, as eluent. The pure fractions were collected and the eluent was evaporated. The residue solidified slowly and the solid product was suspended in 2,2'-oxybispropane. The product was filtered off and dried at the air, yielding 6 parts of cis-1-(1H-benzimidazol-2-ylmethyl)-3-methoxy-4-piperidinamine dihydrate; mp. 92.0° C. (intermediate 122).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05057525 |
|---|
| Source dataset | uspto-grants-1991_10 |
|---|
| ORD ID | ord-c35d9cd0849f402fb7f7bd5972f33587 |
|---|
| Source note | uspto-grants-1991_10 |
|---|