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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184439Generated: October 30, 2026

Sodium Carbonate → 3-(2-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)benzoic acid

https://huagongshe.com/reaction/1184439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Carboxyphenylboronic acidHCID 2733957—
Reactant6-bromo-2-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 22622903—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product3-(2-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)benzoic acidHCID 66716846—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 20 mL screw cap vial was added 6-bromo-2-methyl-2H-benzo[b][1,4]oxazin-3(4H)-one 19 (100 mg, 0.5 mmol), 3-carboxy phenylboronic acid (91 mg, 0.55 mmol), Pd(PPh3)4 (17 mg, 0.015 mmol), and aqueous Na2CO3 (2M, 0.62 mL, 1.25 mmol) in DMF (4 mL). The reaction was heated at 80° C. overnight then cooled and filtered. The filtrate was purified by preparative HPLC-MS (15-60% MeCN in water). The appropriate fractions were combined and concentrated in vacuo to give a white solid: 1H NMR (DMSO-d6, 400 MHz): δ=13.11 (br. s., 1H), 10.72 (s, 1H), 8.09 (t, J=1.6 Hz, 1H), 7.91 (dt, J=7.6, 1.4 Hz, 1H), 7.80-7.85 (m, 1H), 7.54-7.62 (m, 1H), 7.27 (dd, J=8.3, 2.3 Hz, 1H), 7.20 (d, J=2.0 Hz, 1H), 7.07 (d, J=8.3 Hz, 1H), 4.69-4.77 (m, 1H), 1.45 ppm (d, J=6.8 Hz, 3H). ESI-MS: m/z 284.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669249B2
Source datasetuspto-grants-2014_03
ORD IDord-a549681dd31849498424d71e2d06a67d
Source noteuspto-grants-2014_03