HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378236Generated: November 1, 2026
2-Azetidinecarboxylic acid, (S)- → HCID 54138438, compound
https://huagongshe.com/reaction/1378236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Azetidinecarboxylic acid, (S)- | HCID 16486 | — |
| Reactant | 5-Chloroisatoic anhydride | HCID 78480 | — |
| Solvent | acetic acid N,N-dimethylformamide | HCID 21926011 | — |
| Product | HCID 54138438 | HCID 54138438 | 86.3% |
Reaction Steps
59.3 g (0.3 mol) of 5-chloro-isatoic anhydride and 30.3 g (0.3 mol) of (S)-azetidine-2-carboxylic acid were suspended in 400 ml of N,N-dimethylformamide/acetic acid 5:1 and heated to 87°-90° in an oil bath under argon for 64 hrs. The solvent was removed in a vacuum and the residue was taken up in 500 ml of methanol, whereupon the mixture was stirred at room temperature for 30 min. The white, pure crystals were filtered off under suction. The solvent was removed in a vacuum and the semi-crystalline residue was recrystallized from 60 ml of methanol (hot filtration). The products were combined and dried in a vacuum. There were obtained 61.3 g (86%) of (S)-6-chloro-1,2,4,9,10,10a-hexahydro-azeto[2,1-c][1,4]benzodiazepine-4,10-dione of m.p. 229°-231° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665718 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-bd419b93a0f644f38694c4e5ed78ff1f |
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| Source note | uspto-grants-1997_09 |
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