HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178502062, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N1-(1-benzylpiperidin-4-yl)benzene-1,2-diamine | HCID 93779 | — |
| Reactant | Methyl (iminomethoxymethyl)-carbamate | HCID 15037334 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178502062 | HCID 178502062 | — |
Reaction Steps
A mixture of 5 parts of N-[1-(phenylmethyl)-4-piperidinyl]-1,2-benzenediamine, 2.35 parts of methyl (iminomethoxymethyl)carbamate, 5 parts of acetic acid and 75 parts of trichloromethane is stirred and refluxed for 48 hours. The reaction mixture is evaporated and the residue is taken up in water. The solution is neutralized with ammonium hydroxide solution. The precipitated product is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 1.75 parts of methyl {1,3-dihydro-1-[1-(phenylmethyl)-4-piperidinyl]-2H-benzimidazol-2-ylidene}carbamate; mp. 169.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04031226 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-85b2724c332741d8b0abd71422084ed1 |
| Source note | uspto-grants-1977_06 |