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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965983Generated: November 1, 2026

HCID 68856700, compound → HCID 59787401, compound

https://huagongshe.com/reaction/1965983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68856700HCID 68856700—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 59787401HCID 59787401—

Reaction Steps

Dissolve 3-tert-butoxycarbonyl-7-chloro-6-[5-(cyclopentanecarbonyl-amino)-pent-1-enyl]-2,3,4,5-tetrahydro-1H-benzo[d]azepine as obtained in the previous step in EtOAc (20 mL) and add 10% Pd/C (Degussa type, 200 mg). Then apply a pressure of 70 psi of hydrogen while shaken vigorously. Filter the crude mixture through a short pad of Celite® and concentrate in vacuo. Purify the resulting material by preparative HPLC to obtain the desired intermediate as a clear oil (311 mg, 87% for the two previous steps). MS (ES+) m/z=485.2 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420631B2
Source datasetuspto-grants-2013_04
ORD IDord-1a4e078b608246ac8c7a47442ff3c434
Source noteuspto-grants-2013_04