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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519035Generated: October 29, 2026

HCID 86727396, compound → HCID 86727398, compound

https://huagongshe.com/reaction/519035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86727396HCID 86727396—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86727398HCID 8672739895%

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)-3-methyl-azetidine-1-carboxylic acid tert-butyl ester (0.054 g, 0.122 mmol) and Pd/C (10%, 0.015 g) 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)-3-methyl-azetidine-1-carboxylic acid tert-butyl ester as a white solid (0.049 g, 95%). LC/MS (Table 1, Method 2) Rt=1.327 min.; MS m/z: 467 [M+23]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-17149e991ebc431ab0bc9f1bff4d9ef4
Source noteuspto-grants-2015_08