Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Azetidinecarboxylic acid, (S)-HCID 16486—
Reactant5-Chloroisatoic anhydrideHCID 78480—
Solventacetic acid N,N-dimethylformamideHCID 21926011—
ProductHCID 54138438HCID 5413843886.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-bd419b93a0f644f38694c4e5ed78ff1f
Source noteuspto-grants-1997_09