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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969687Generated: November 4, 2026

Anthranilic Acid → 2-amino-N-(4-tert-butylphenyl)benzamide

https://huagongshe.com/reaction/969687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
Reactant4-Tert-ButylanilineHCID 69861—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-amino-N-(4-tert-butylphenyl)benzamideHCID 335177—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 4-tert-butyl-phenylamine (5.8 mL, 36.5 mmol), 2-amino-benzoic acid (5.0 g, 36.5 mmol), TBTU (12.9 g, 40.2 mmol) and DIEA (6.7 mL, 40.2 mmol) in 5 mL of DMF was heated (50° C.) for 12 h in a sealed tube. The mixture was diluted with EtOAc and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography (SiO2, 20% EtOAc/hexane) and crystallized from EtOH:H2O (3:1) to afford a yellow solid. MS (ES+): 269.4. (M+H)+. Calc'd for C17H20N2O-268.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307088B2
Source datasetuspto-grants-2007_12
ORD IDord-e6b994e230c646c7b02fd7b05b3621ba
Source noteuspto-grants-2007_12