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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518998Generated: November 2, 2026

HCID 86727352, compound → HCID 86727353, compound

https://huagongshe.com/reaction/518998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86727352HCID 86727352—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86727353HCID 8672735353.1%

Reaction Steps

A suspension of 3-(7-isopropenyl-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yloxy)-azetidine-1-carboxylic acid tert-butyl ester (0.030 g, 0.070 mmol) and 10% Pd/C (10 mg) in MeOH (10 mL) was stirred under H2 (50 psi) at ambient temperature overnight. The reaction mixture was filtered and the filtrate was evaporated in vacuo. The residue was purified by preparative TLC (eluting with 30% EtOAc in petroleum ether) to give 3-(7-isopropyl-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yloxy)-azetidine-1-carboxylic acid tert-butyl ester as a white solid (0.016 g, 53%). LC/MS (Table 1, Method 2) Rt=1.275 min.; MS m/z: 431 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-759358caa3554a65b702981d4cb79004
Source noteuspto-grants-2015_08