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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623849Generated: October 25, 2026

2-Amino-6-nitro-benzoic acid → 2-methyl-5-nitro-4H-benzo[d][1,3]oxazin-4-one

https://huagongshe.com/reaction/623849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-nitro-benzoic acidHCID 95795—
ReactantAvadomideHCID 24967599—
SolventAcetic AcidHCID 176—
Product2-methyl-5-nitro-4H-benzo[d][1,3]oxazin-4-oneHCID 66642983—

Reaction Steps

In yet another embodiment, provided herein is a method for preparing 3-(5-amino-2-methyl-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione, or an enantiomer or a mixture of enantiomers thereof or a pharmaceutically acceptable salt, solvate, hydrate, or polymorph thereof; comprising the steps of (a) reacting 2-amino-6-nitrobenzoic acid with an activated acetic acid in a solvent to form 2-methyl-5-nitro-4H-benzo[d][1,3]oxazin-4-one; (b) reacting 2-methyl-5-nitro-4H-benzo[d][1,3]oxazin-4-one with 3-aminopiperidine-2,6-dione or a salt thereof in a solvent to form 3-(2-methyl-5-nitro-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione; and (c) reducing 3-(2-methyl-5-nitro-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione in a solvent to form 3-(5-amino-2-methyl-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione, or an enantiomer or a mixture of enantiomers thereof or a pharmaceutically acceptable salt, solvate, hydrate, or polymorph thereof.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303014B2
Source datasetuspto-grants-2016_04
ORD IDord-ab7e29518922425b9a462ed560f3b836
Source noteuspto-grants-2016_04