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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409617Generated: November 1, 2026

Imidazole → HCID 66642839, compound

https://huagongshe.com/reaction/1409617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriphenyl phosphiteHCID 7540—
Reactant2-methyl-5-nitro-4H-benzo[d][1,3]oxazin-4-oneHCID 66642983—
ReactantHCID 66643204HCID 66643204—
SolventDimethylformamideHCID 6228—
ProductHCID 66642839HCID 6664283919%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 2-methyl-5-nitro-4H-benzo[d][1,3]oxazin-4-one (2.0 g, 9.7 mmol), (R)-3-amino-3-methylpiperidine-2,6-dione hydrobromide (2.2 g, 9.7 mmol), imidazole (1.5 g, 21 mmol), and triphenylphosphite (3.7 g, 12 mmol) in DMF (20 mL) was stirred under nitrogen at 45° C. for 40 hours. The mixture was evaporated, and the residue was chromatographed on silica gel using a dichloromethane-acetonitrile gradient. The product eluted at 60% acetonitrile, providing (R)-3-methyl-3-(2-methyl-5-nitro-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione as a yellow solid (0.60 g, 19% yield); 1H NMR (DMSO-d6) δ 1.94 (s, 3H, CH3), 2.35-2.40 (m, 1H, CHH), 2.45-2.59 (m, 2H, 2CHH), 2.71-2.83 (m, 4H, CH3, CHH), 7.75-7.82 (m, 2H, Ar), 7.95 (dd, J=8, 8 Hz, 1H, Ar), 10.86 (s, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921385B2
Source datasetuspto-grants-2014_12
ORD IDord-47765a8f32f1405dba7fe617d4e3bccb
Source noteuspto-grants-2014_12