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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259842Generated: November 1, 2026

6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one → HCID 67223394, compound

https://huagongshe.com/reaction/1259842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 2763681—
ReactantHCID 11217932HCID 11217932—
SolventWater ethanolHCID 19096565—
ProductHCID 67223394HCID 6722339440.2%

Reaction Steps

A solution of 6-amino-4H-benzo[1,4]oxazin-3-one (commercial; 6.49 g, 39.5 mmol) and (2R)-tert-butyl-dimethyl-(2-oxiranyl-ethoxy)-silane (first eluting compound of step 18.i, 8.0 g, 39.5 mmol) in 9-1 EtOH/H2O (240 mL) was heated at 80° C. for 2 days. The mixture was concentrated under reduced pressure. Residual starting aniline could be removed by addition of Et2O/MeOH followed by filtration. The filtrate was concentrated under reduced pressure and the residue was purified by CC (DCM/MeOH/NH4OH 1000:50:4) to afford the title intermediate as a brown oil (5.82 g, 40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466168B2
Source datasetuspto-grants-2013_06
ORD IDord-5fd721eb8c1f46fdaba171948362f7d5
Source noteuspto-grants-2013_06