Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602873Generated: October 29, 2026

HCID 66923012, compound → (S)-3-(4-Hydroxy-phenyl)-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester

https://huagongshe.com/reaction/602873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66923012HCID 66923012—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(S)-3-(4-Hydroxy-phenyl)-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl esterHCID 66922983—

Reaction Steps

To a solution of (S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester (1 mmol) in methanol was added Pd/C (0.2 mmol). The mixture was hydrogenated using balloon for 2-4 h. The mixture was passed through a pad of celite and the filtrate was evaporated to furnish (S)-3-(4-Hydroxy-phenyl)-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester. This ester was converted to (S)-7-[(S)-2-(4′-Cyano-biphenyl-4-yl)-1-methoxycarbonyl-ethylcarbamoyl]-3-(4-hydroxy-phenyl)-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6-carboxylic acid tert-butyl ester using the general procedure A. LC-MS (m/z): 704.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906507B2
Source datasetuspto-grants-2011_03
ORD IDord-3cba579759804591b788c1ab5ca6b99a
Source noteuspto-grants-2011_03