Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499609Generated: November 1, 2026

HCID 86726828, compound → HCID 86726827, compound

https://huagongshe.com/reaction/1499609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86726828HCID 86726828—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 86726827HCID 86726827100%

Reaction Steps

A solution of 4-{(3R,4R,5S)-4-(acetyloxy)-3-[(tert-butoxycarbonyl)amino]-5-cyclopropylpiperidin-1-yl}-3-nitro-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl acetate (0.055 g, 0.11 mmol) in MeOH (5.0 mL) and EtOAc (1.0 mL) was deoxygenated and purged with nitrogen prior to the addition of 10% palladium (dry basis) on activated carbon (wet, Degussa type E101 NE/W) (0.025 g). The reaction mixture was stirred under an atmosphere of hydrogen, introduced via a balloon, for 2 h. The crude reaction mixture was filtered through a pad of diatomaceous earth and the solids were washed thoroughly with EtOAc and MeOH. The filtrate was concentrated under reduced pressure to afford the sub-title compound (0.052 g, 100%). LCMS (ESI) m/z calc. for C25H37N4O6 489.3 [M+H]+. found 489.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-d17f9ad824d040b09ad19641fe7bb15c
Source noteuspto-grants-2015_12