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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519007Generated: October 30, 2026

HCID 86727363, compound → HCID 86727365, compound

https://huagongshe.com/reaction/519007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86727363HCID 86727363—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86727365HCID 86727365100%

Reaction Steps

To a solution of 4-(4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (1.1 g, 2.76 mmol) in MeOH (15 mL) was added Pd/C (10%, 0.110 g) and the reaction mixture was stirred under H2 (1 atm) for 10 h. The catalyst was removed by filtration, washing with methanol (3×5 mL). The filtrate was concentrated in vacuo to give 4-(4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yl)-piperidine-1-carboxylic acid tert-butyl ester (1.05 g, 100%). LC/MS (Table 1, Method 3) Rt=1.428 min.; MS m/z: 401 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-275d87f76b414c45b43751a81ac3687e
Source noteuspto-grants-2015_08