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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383428Generated: October 26, 2026

Pyridine → N-(2-bromo-4-methyl-phenyl)-6-(trifluoromethoxy)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide

https://huagongshe.com/reaction/383428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Bromo-4-methylanilineHCID 11422—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant6-(trifluoromethoxy)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylic acidHCID 59394962—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductN-(2-bromo-4-methyl-phenyl)-6-(trifluoromethoxy)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamideHCID 5939493976%

Reaction Steps

6-(Trifluoromethoxy)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylic acid (600 mg, 2.28 mmol) and 2-bromo-4-methyl-aniline (424 mg, 286 μL, 2.28 mmol) were dissolved in 2-methyltetrahydrofuran (7 mL) and pyridine (461 μL, 5.70 mmol). T3P (2902 mg, 2.7 mL of 50% w/w solution, 4.56 mmol) was added and the reaction was stirred for 30 min at room temperature. Purification by silica gel chromatography (10-100% ethyl acetate/hexanes) provided N-(2-bromo-4-methylphenyl)-6-(trifluoromethoxy)-3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxamide (743 mg, 76% yield). LC/MS m/z 432.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367660B2
Source datasetuspto-grants-2013_02
ORD IDord-acfbd79d71e648c7b72f8b46a7362ed6
Source noteuspto-grants-2013_02