HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580604Generated: November 1, 2026
Clonazepam → 7-nitro-2,3-dihydro-2-oxo-5-(o-chlorophenyl)-1H-1,4-benzodiazepin-1-acetic acid propyl ester
https://huagongshe.com/reaction/1580604
Participants
| Role | Name | HCID | Charge |
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| Reactant | Clonazepam | HCID 2802 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Acetic acid, bromo-, propyl ester | HCID 141981 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-nitro-2,3-dihydro-2-oxo-5-(o-chlorophenyl)-1H-1,4-benzodiazepin-1-acetic acid propyl ester | HCID 53926365 | — |
Reaction Steps
A mixture of 0.1 mole of 7-nitro-1,3-dihydro-5-(o-chlorophenyl)-2H-1,4-benzodiazepin-2-one and 0.11 mole of sodium methoxide in about 200 ml. of dimethylformamide is heated at about 95° C. for about 20 minutes. To the mixture is added a solution of 0.11 mole of propyl bromoacetate in about 200 ml. of toluene over a period of about 1 hour at about 95° C., and heating is continued for an additional period of about 6 hours. The reaction mixture is then evaporated in vacuo and the residue thus obtained is stirred with about 500 ml. of water. The resulting suspension is filtered and the solids thus obtained are crystallized from a suitable organic solvent such as ether, methanol, methylene chloride, methylene chloride-methanol and the like to obtain 7-nitro-2,3-dihydro-2-oxo-5-(o-chlorophenyl)-1H-1,4-benzodiazepin-1-acetic acid propyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03933816 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-51424b6e3056469693ac861280213e33 |
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| Source note | uspto-grants-1976_01 |
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