Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Bromopropylamine hydrobromide | HCID 78701 | — |
| Reactant | 1-(4-fluorophenylmethyl)-N-[1-(2-isothiocyanatoethyl)-4-piperidinyl]1H-benzimidazol-2-amine | HCID 12891753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22932077 | HCID 22932077 | — |
Reaction Steps
A mixture of 2.2 parts of 3-bromo-1-propanamine hydrobromide, 4.1 parts of 1-[(4-fluorophenyl)methyl]-N-[1-(2-isothiocyanatoethyl)-4-piperidinyl]-1H-benzimidazol-2-amine, 2.2 parts of sodium carbonate and 135 parts of tetrahydrofuran was stirred overnight at room temperature. The reaction mixture was further stirred and refluxed for 3 hours. The mixture was filtered and the filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume), saturated with ammonia, as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile, yielding 2.5 parts of 1-[(4-fluoro-phenyl)methyl]-N-[1-[2-[(5,6-dihydro-4H-1,3-2-yl)amino]ethyl]-4-piperidinyl[-1H-benzimidazol-2-amine monohydrate; mp 121.4° C. (compound 117).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE033833 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-af77be1749fa44a5ac7031e8710fbdd2 |
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| Source note | uspto-grants-1992_02 |
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