Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | HCID 86755705 | HCID 86755705 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86755704 | HCID 86755704 | 33.5% |
Reaction Steps
Isatoic anhydride (0.49 g) was added to a mixture of (±)-trans-1-(2-ethoxyethyl)-N-[2-(phenylmethyl)-4-piperidinyl]-1H-benzimidazol-2-amine (1.14 g) in CH2Cl2 (150 ml), the mixture was stirred for 3 hours and then refluxed for 3 hours. The solvent was evaporated, 2-propanol (100 ml) was added to the residue and the mixture was refluxed for 18 hours. Isatoic anhydride (0.2 g) was added again and the mixture was refluxed for 4 hours. The solvent was evaporated and the residue was purified by column chromatography over silica gel (eluent: CH2Cl2 /CH3OH 95/5). The pure fractions were collected and evaporated. The residue was crystallized from DIPE, yielding 0.5 g (33.4%) of (±)-trans-1-[2-aminobenzoyl]-4-[[1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]amino]-2-(phenylmethyl)piperidine (comp 123; mp. 197.4° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06110939 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-a83e441195e642f49b74b02ea4820a3b |
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| Source note | uspto-grants-2000_08 |
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