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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64822Generated: October 29, 2026

(S)-N-Butylpyrrolidine-2-carboxamide → HCID 178449505, compound

https://huagongshe.com/reaction/64822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-N-Butylpyrrolidine-2-carboxamideHCID 22691332—
ReactantHCID 178514453HCID 178514453—
ReactantN-cbz-l-histidyl azideHCID 178514642—
SolventEthyl AcetateHCID 8857—
ProductHCID 178449505HCID 178449505—

Reaction Steps

To 75 ml of an ethyl acetate solution of Nα -benzyloxycarbonyl-L-histidine azide (4) prepared from 4.85 g of Nα -benzyloxycarbonyl-L-histidine hydrazide (3) by the method of Reference example 2 was added 2.23 g of compound (31) under ice-cooling and the mixture was placed overnight in a refrigerator to complete the reaction. The reaction mixture was concentrated and the residue was subjected to silica gel column chromatography. By eluting the product with chloroform-methanol-aqueous ammonia (95:5:0.5), 4.13 g of Nα -benzyloxycarbonyl-L-histidyl-N-butyl-L-prolinamide was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04610821
Source datasetuspto-grants-1986_09
ORD IDord-e9c8a3fc903b42bfbfd38a0591a1a898
Source noteuspto-grants-1986_09