Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | N-(2-benzoylphenyl)-2-chloroacetamide | HCID 2064069 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | RO-05-2921 | HCID 76175 | 84.7% |
Reaction Steps
Paraformaldehyde (200 g., 91% flake) is placed in a stirred reactor equipped with a reflux condenser, decanter, and ammonia addition tube. Methanol (575 mls.) is added and then gaseous ammonia below the surface of the reaction mixture. 2-Chloroacetamido-benzophenone (273.7 g.) is then added. With a slow, continuous flow of ammonia to the reaction zone, the mixture is heated at reflux for 5 hours. The crystal slurry obtained is distilled to recover the methanol. Toluene (1350 mls.) is now added to the crystal residue and residual water is removed by azeotropic distillation through the decanter. When dry, the hot toluene solution is filtered, the filtrate is cooled for crystallization, and the product obtained isolated to give 1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one (200 g., 84.7%) m.p. 180°-181° C. (uncorr.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03996209 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-4caa97eb1a444f299db8130eb2318f7b |
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| Source note | uspto-grants-1976_12 |
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