HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580607Generated: October 30, 2026
Bromazepam → 7-bromo-2,3-dihydro-2-oxo-alpha-propyl-5-(2-pyridyl)-1H-1,4-benzodiazepine-1-acetic acid methyl ester
https://huagongshe.com/reaction/1580607
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromazepam | HCID 2441 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl 2-bromopentanoate | HCID 529992 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-bromo-2,3-dihydro-2-oxo-alpha-propyl-5-(2-pyridyl)-1H-1,4-benzodiazepine-1-acetic acid methyl ester | HCID 54389182 | — |
Reaction Steps
A mixture of 0.1 mole of 7-bromo-1,3-dihydro-5-(2-pyridyl)-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 methyl 2-bromovalerate 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-bromo-2,3-dihydro-2-oxo-α-propyl-5-(2-pyridyl)-1H-1,4-benzodiazepine-1-acetic acid methyl 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-c162350d230341889fa0982c0460e1bc |
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| Source note | uspto-grants-1976_01 |
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