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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038813Generated: October 30, 2026

2,2-difluoro-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-one → 6-amino-2,2-difluoro-2H-benzo[b][1,4]oxazin-3(4H)-one

https://huagongshe.com/reaction/1038813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-difluoro-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-oneHCID 59410534—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product6-amino-2,2-difluoro-2H-benzo[b][1,4]oxazin-3(4H)-oneHCID 2206114666.4%

Reaction Steps

In a flask, 10% Pd/C (0.819 g, 0.769 mmol) was added. The flask was placed under vacuum and purged with N2 three times and then MeOH (25 mL) was added. To the flask was added a solution of 2,2-difluoro-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-one (5.90 g, 25.6 mmol, WO2008024634A1, Page 161, Intermediate C) in MeOH (20 mL). The mixture was then evacuated, purged with N2 and evacuated again. The mixture was placed under an atmosphere of H2 and stirred at rt for about 16 h. The mixture was placed under vacuum and purged with N2 three times. The mixture was filtered over a Celite Pad®, washed with MeOH (300 mL) and concentrated under reduced pressure to give 6-amino-2,2-difluoro-2H-benzo[b][1,4]oxazin-3(4H)-one (3.4 g, 66%); LC/MS (Table 2, Method c) Rt=1.42 min.; MS m/z: 201 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551981B2
Source datasetuspto-grants-2013_10
ORD IDord-4302671c27ad4653b0d83ee9a30cbf28
Source noteuspto-grants-2013_10