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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647862Generated: October 30, 2026

HCID 54045935, compound → HCID 13243524, compound

https://huagongshe.com/reaction/647862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54045935HCID 54045935—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 13243524HCID 13243524—

Reaction Steps

A solution of 5-acetoxy-3-(S)-t-butyloxycarbonylamino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one (0.7 g) in ethanol (50 ml) was hydrogenated at 42 psi for 24 hours at 70° using 10% palladium on charcoal (0.5 g) as catalyst. The catalyst was filtered off and the solvent removed under reduced pressure to give 3-(S)-t-butyloxycarbonylamino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one which, without further purification was converted to 3-(S)-amino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one by the procedure described above; m.p. 99°-101°, [α]D =-297° (c=1 in ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410520
Source datasetuspto-grants-1983_10
ORD IDord-cd8ea3574b74423facf30a99076cafc9
Source noteuspto-grants-1983_10