HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Azetidinecarboxylic acid, (S)- → (S)-5-bromo-1,10a-dihydroazeto[2,1-c][1,4]benzodiazepine-4,10(2H,9H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Azetidinecarboxylic acid, (S)- | HCID 16486 | — |
| Reactant | 5-bromo-2,4-dihydro-1H-3,1-benzoxazine-2,4-dione | HCID 10752644 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (S)-5-bromo-1,10a-dihydroazeto[2,1-c][1,4]benzodiazepine-4,10(2H,9H)-dione | HCID 54191878 | — |
Reaction Steps
25 g (103 mmol) of 6-bromo-isatoic acid anhydride and 10.44 g (103 mmol) of L-azetidine-2-carboxylic acid in 100 ml of dimethyl sulphoxide are stirred at 95° for 25 minutes, the dimethyl sulphoxide is removed in vacuo and the residue is heated to 150° for 3 hours in a high vacuum. By chromatography of the resulting material on silica gel while eluting with ethyl acetate and subsequent recrystallization from ethyl acetate there is obtained (S)-5-bromo-1,10a-dihydroazeto[2,1-c][1,4]benzodiazepine-4,10(2H,9H)-dione of melting point 182°-183°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04489003 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-04b63728ee274a389c37fd6e0984ea5a |
| Source note | uspto-grants-1984_12 |