HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Azetidinecarboxylic acid, (S)- → HCID 53806438, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Azetidinecarboxylic acid, (S)- | HCID 16486 | — |
| Reactant | 6-(Iodo)isatoic anhydride | HCID 10684815 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 53806438 | HCID 53806438 | — |
Reaction Steps
70 g (242 mmol) of 6-iodoisatoic acid anhydride and 24.46 g (242 mmol) of L-azetidine-2-carboxylic acid in 140 ml of dimethyl sulphoxide are stirred at 105° for 2 hours, the dimethyl sulphoxide is removed in vacuo and the residue is heated to 140° in a high vacuum for 2.5 hours. By chromatography on silica gel while eluting with ethyl acetate and subsequent recrystallization from ethyl acetate there is obtained (S)-1,10a-dihydro-5-iodo-azeto[2,1-c][1,4]benzodiazepine-4,10(2H,9H)-dione of melting point 186°-187°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04489003 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-317e3562a2d94f11b76650e6521fc98a |
| Source note | uspto-grants-1984_12 |