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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099967Generated: October 27, 2026

Triethylamine → Methyl 4-((2-(isopropylcarbamoyl)-4-phenoxyphenyl)carbamoyl)benzoate

https://huagongshe.com/reaction/2099967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMonomethyl terephthalateHCID 15513—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-amino-N-isopropyl-5-phenoxybenzamideHCID 57796894—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-((2-(isopropylcarbamoyl)-4-phenoxyphenyl)carbamoyl)benzoateHCID 5779690185%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 34C (72 mg, 0.27 mmol) in DMF (4 mL) was treated with 4-(methoxycarbonyl)benzoic acid (78 mg, 0.43 mmol), HOBt (66 mg, 0.43 mmol) and triethylamine (100 mg, 1.0 mmol). The solution was treated with EDCI (96 mg, 0.5 mmol) at room temperature for 15 minutes, and then warmed to 65° C. for 16 hours. The reaction mixture was partitioned between EtOAc (20 mL) and 1 M HCl (20 mL). The organic layer was washed with 1 N HCl (20 mL), 1 N NaOH (20 mL) and brine (20 mL). The reaction was dried (Na2SO4), filtered, and concentrated to a solid. The crude material was purified by chromatography (SiO2, 1:2 EtOAc in heptane) to afford 34D (99 mg, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569725B2
Source datasetuspto-grants-2009_08
ORD IDord-939636c2a5a84e6ab04a867776e6bd59
Source noteuspto-grants-2009_08