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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485186Generated: October 30, 2026

Hydrochloric Acid → HCID 131713676, compound

https://huagongshe.com/reaction/485186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantHCID 131713677HCID 131713677—
ReactantHCID 131713678HCID 131713678—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventButanol acetic acid waterHCID 22056973—
ProductHCID 131713676HCID 131713676—

Reaction Steps

1-[N-[3-(Benzoylamino)-7-[[(phenylmethoxy)carbonyl]amino]-2-oxoheptyl]-N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-proline, phenylmethyl ester (1.3 g., 1.6 mmole) is dissolved in ethanol (75 ml.) and aqueous hydrochloric acid (1N, 5 ml.). Palladium on carbon catalyst (10%, 450 mg.) is added and the mixture is hydrogenated at atmospheric pressure overnight. The catalyst is filtered off and the solution is evaporated in vacuo. The residue is dissolved in water and lyophilized. The lyophilate is triturated with ether to give 0.6 g. of 1-[N-[7-amino-3-(benzoylamino)-2-oxoheptyl]-L-alanyl]-L-proline, hydrochloride; m.p. 80°-155°; [α]D22 =-50° (c=1.1, methanol). Rf 0.09 (silica gel, n-butanol/acetic acid/water, 4:1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535176
Source datasetuspto-grants-1985_08
ORD IDord-638d9cfd098841df9ea8045a7fa638a4
Source noteuspto-grants-1985_08