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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519013Generated: October 30, 2026

HCID 86727369, compound → HCID 86727370, compound

https://huagongshe.com/reaction/519013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86727369HCID 86727369—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86727370HCID 86727370100%

Reaction Steps

To a solution of 4-(7-isopropenyl-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 (0.035 g, 2.76 mmol) in MeOH (15 mL) was added Pd/C (10%, 0.005 g, 0.005 mmol). The reaction mixture was stirred under an H2 atmosphere (50 psi) for 10 h. The catalyst was removed by filtration and washed with methanol (3×5 mL). The filtrate was concentrated in vacuo to give 4-(7-isopropyl-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 (0.035 g, 100%). LC/MS (Table 1, Method 5) Rt=3.554 min.; MS m/z: 443 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-774b40bd552a4e349010cbbba4112adb
Source noteuspto-grants-2015_08