HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67430Generated: October 28, 2026
Carbon Dioxide → 7-Bromo-4-methyl-3,4-dihydro-1H-benzo[E][1,4]diazepine-2,5-dione
https://huagongshe.com/reaction/67430
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sarcosine | HCID 1088 | — |
| Reactant | 5-Bromoisatoic Anhydride | HCID 288561 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 7-Bromo-4-methyl-3,4-dihydro-1H-benzo[E][1,4]diazepine-2,5-dione | HCID 5297644 | — |
Reaction Steps
A solution of 39.5 g of 5-bromoisatoic acid anhydride and 14.5 g of sarcosine in 150 ml of dimethyl sulphoxide is heated to 100° C. while stirring. In so doing, a vigorous evolution of carbon dioxide occurs from 70° C. and this has finished after ca 30 minutes. The mixture is stirred at 100° C. for a further 30 minutes and thereafter the mixture is poured into 900 ml of ice-water (temperature 5° C.) and the separated material is filtered off under suction. The crystals are washed with water and subsequently dried at 50° C. over phosphorus pentoxide in a vacuum drying cabinet. There is obtained 7-bromo-3,4-dihydro-4-methyl-2H-1,4-benzodiazepine-2,5(1H)-dione in the form of light beige crystals. A sample recrystallised from methanol has a melting point of 260°-261° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04346032 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-45ee802dff6147148c3a3fa4f1438be5 |
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| Source note | uspto-grants-1982_08 |
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