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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354978Generated: November 1, 2026

Anthranilamide → HCID 13521076, compound

https://huagongshe.com/reaction/1354978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilamideHCID 6942—
Reactant2-ChlorotolueneHCID 7238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product2-amino-N-(2-methylphenyl)benzamideHCID 72085510%
ProductHCID 13521076HCID 1352107687%

Reaction Steps

An oven-dried resealable schlenk tube containing a stir bar was charged with Pd2(dba)3 (4.6 mg, 0.005 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (19.0 mg, 0.04 mmol), 2-aminobenzamide (170 mg, 1.25 mmol) and K2CO3 (173 mg, 1.25 mmol). The tube was capped with a rubber septum, evacuated and backfilled with argon. 2-Chlorotoluene (60 μL, 0.5 mmol) and tbutanol (1 mL) were added through the septum via syringe. The septum was replaced with a Teflon screw cap. The schlenk tube was sealed and put into a pre-heated oil bath at 110° C. The reaction mixture was stirred for 17 h, allowed to cool down to room temperature and filtered through celite with ethyl acetate. The filtrate was concentrated under reduced pressure. Chromatography on silica gel column with 4:1 hexane:ethyl acetate gave 98 mg (87%) of 2-(2-methylphenylamino)benzamide as a white solid and 11 mg (10%) of 2-amino-N-(2-methylphenyl)benzamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223879B2
Source datasetuspto-grants-2007_05
ORD IDord-a6ae417b06e74d4aba38c4df9f724ff2
Source noteuspto-grants-2007_05