Participants
| Role | Name | HCID | Charge |
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| Reactant | Urea | HCID 1176 | — |
| Reactant | HCID 21500251 | HCID 21500251 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21500249 | HCID 21500249 | — |
Reaction Steps
A mixture of 36 parts of methyl 4-(2-amino-4-chlorophenylamino)-2-methyl-1-piperidinecarboxylate and 14 parts of urea is stirred and heated in an oil-bath at 160° C. for 4 hours. After cooling, the reaction mixture is disslved in methylbenzene. The solution is washed successively three times with water, twice with a diluted hydrochloric acid solution and again three times with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silicagel, using trichloromethane as eluent. The pure fractions are collected and the eluent is evaporated, yielding methyl 4-(5-chloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)-2-methyl-1-piperidinecarboxylate as an oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03989707 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-864f4c2a6ee04fec9a415680487f5bfb |
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| Source note | uspto-grants-1976_11 |
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