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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77768Generated: October 26, 2026

Ethylamine → 5-Ethylcarbamoyl-4'-methyl-biphenyl-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/77768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantTetrahydrofuranHCID 8028—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5-Iodo-4'-methyl-biphenyl-3-carboxylic acid methyl esterHCID 57851588—
Catalystpalladium(II) acetateHCID 167845—
Product5-Ethylcarbamoyl-4'-methyl-biphenyl-3-carboxylic acid methyl esterHCID 5785162750%

Reaction Steps

A 20 mL of vial was charged with 5-iodo-4′-methyl-biphenyl-3-carboxylic acid methyl ester (500 mg, 1.42 mmol), Pd(OAc)2 (9.6 mg, 0.043 mmol), Mo(CO)6 (413.5 mg, 1.566 mmol), ethylamine (2.0 M in MeOH, 1.068 mL, 2.136 mmol), DBU (426 uL, 2.848 mmol) and dry THF (10 mL). The vial was immediately capped with a Teflon septum under air and irradiated with microwaves to 100° C. for 15 minutes. After cooling, the reaction mixture was filtered through a short celite pad and the solvent, and excess DBU was removed under reduced pressure. The residue was purified by preparative HPLC to afford 210 mg of 5-ethylcarbamoyl-4′-methyl-biphenyl-3-carboxylic acid methyl ester (yield 50%). MS (M+H)=298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841336B2
Source datasetuspto-grants-2014_09
ORD IDord-71dc9730ee74456baebc7b305f55d071
Source noteuspto-grants-2014_09