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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515510Generated: October 25, 2026

3,4-Dimethoxyphenylboronic acid → 2-(3-Carbamoyl-4-fluorophenylamino)-2-(3,4-dimethoxyphenyl)acetic acid

https://huagongshe.com/reaction/1515510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethoxyphenylboronic acidHCID 2734702—
Reactant5-Amino-2-fluorobenzamideHCID 2778899—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product2-(3-Carbamoyl-4-fluorophenylamino)-2-(3,4-dimethoxyphenyl)acetic acidHCID 5947939246%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-amino-6-fluorobenzamide (85 mg, 0.5 mmol), 3,4-dimethoxyphenylboronic acid (91 mg, 0.5 mmol) and glyoxylic acid monohydrate (46 mg, 0.5 mmol) in acetonitrile (2.0 mL) and DMF (0.2 mL) was heated at 100° C. for 20 min. in a microwave reactor. After removal of solvent, the crude was triturated with methylene chloride. The precipitate formed was collected by filtration and washed with methylene chloride to give 13A after drying, yield: 46%. 1H NMR (400 MHz, Methanol-d4) δ ppm 3.81 (s, 3H) 3.82 (s, 3H) 4.92 (s, 1H) 6.83-6.89 (m, 1 H) 6.93 (d, J=8.35 Hz, 1H) 6.96-7.02 (m, 1H) 7.03-7.07 (m, 1H) 7.10 (d, J=1.76 Hz, 1H) 7.15 (dd, J=5.93, 2.86 Hz, 1H), LCMS: 349 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222453B2
Source datasetuspto-grants-2012_07
ORD IDord-d0ff8e8dff6a4a3ca256a73b78a79894
Source noteuspto-grants-2012_07