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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413712Generated: November 2, 2026

HCID 70459262, compound → HCID 178475058, compound

https://huagongshe.com/reaction/2413712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70459262HCID 70459262—
ReactantHCID 178513962HCID 178513962—
ProductHCID 178475058HCID 178475058—
ProductHCID 178475059HCID 178475059—

Reaction Steps

The residue containing compound (32) obtained in Reference Example 7 was reacted with L-histidyl-L-prolinamide (free base) in a similar manner as above. The thus obtained reaction mixture was purified by column chromatography using silica gel (150 g). The desired compound was eluted with ethyl acetate-methanol-ammonia water (20:10:1). After the solvent was removed, the product was lyophilized. Thus, 274 mg was obtained as a mixture of Nα -[(2S,3S)-3-acetylamino-4-oxo-2-azetidinylcarbonyl]-L-histidyl-L-prolinamide (34a) and Nα -[(2R,3R)-3-acetylamino-4-oxo-2-azetidinylcarbonyl]-L-histidyl-L-prolinamide (34b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719207
Source datasetuspto-grants-1988_01
ORD IDord-910c2426c29a4bd8bb9ba7f29c116ec2
Source noteuspto-grants-1988_01