HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441484Generated: October 30, 2026
Water → 7-Chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one
https://huagongshe.com/reaction/441484
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Chloro-5-methoxy-1-methyl-4-nitro-5-phenyl-1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-one | HCID 3046726 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one | HCID 3046727 | 44.1% |
Reaction Steps
To a solution of sodium hydride (50% suspension in a mineral oil; 200 mg) in dry dimethylformamide (7.5 ml), 7-chloro-5-methoxy-1-methyl-4-nitro-5phenyl-1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-one (500 mg) is added under cooling at -30° C. and with stirring, and the resultant mixture is stirred at -10° C. for 30 minutes. The reaction mixture is poured into icy water and shaken with diethyl ether. The organic layer is washed with water, dried over sodium sulfate, and evaporated to remove the solvent. The residue is crystallized from diethyl ether to give 7-chloro-5-methoxy-1-methyl-5-phenyl-1,5-dihydro-2H-1,4-benzodiazepin-2-one (192 mg) as colorless prisms melting at 146.5 to 147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04041026 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-1fa956f0e8874173a58464b7d99a8d6b |
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| Source note | uspto-grants-1977_08 |
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