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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373403Generated: October 25, 2026

(3aS,6aR)-hexahydro-1-[(R)-(1-phenylethyl)]-2-oxo-3-benzylthieno[3,4-d]imidazol-4-ylidene pentanoic acid → (3aS,6aR)-hexahydro-1-[(R)-(1-phenylethyl)]-2-oxo-3-benzylthieno-[3,4-d]-imidazol-4-yl pentanoic acid

https://huagongshe.com/reaction/373403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3aS,6aR)-hexahydro-1-[(R)-(1-phenylethyl)]-2-oxo-3-benzylthieno[3,4-d]imidazol-4-ylidene pentanoic acidHCID 86743268—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
Product(3aS,6aR)-hexahydro-1-[(R)-(1-phenylethyl)]-2-oxo-3-benzylthieno-[3,4-d]-imidazol-4-yl pentanoic acidHCID 86743476—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 78.6 mg of (3aS,6aR)-hexahydro-1-[(R)-(1-phenylethyl)]-2-oxo-3-benzylthieno-[3,4-d]-imidazol-4-ylidene pentanoic acid in 5 ml of isopropanol was placed in a 100-ml autoclave and 39 mg of palladium (5 percent) on carbon added. The autoclave was flushed twice with hydrogen and the mixture was stirred under 50 bars of hydrogen pressure at 50° C. for 24 hours. Then the catalyst was filtered off and the solvent evaporated off. The product, (3aS,6aR)-hexahydro-1-[(R)-(1-phenylethyl)]-2-oxo-3-benzylthieno-[3,4-d]-imidazol-4-yl pentanoic acid, was obtained as a colorless oil in a yield of 56.1 mg (72 percent). Concerning the product:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162540
Source datasetuspto-grants-1992_11
ORD IDord-20a0ccdfffc04a3d9954c5fe8657bc37
Source noteuspto-grants-1992_11