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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724158Generated: November 4, 2026

Triethylamine → Furan-3-carboxylic acid N'-[3-(2',3'-dimethyl-biphenyl-2-yl)-propionyl]-N'-isopropyl-hydrazide

https://huagongshe.com/reaction/1724158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-(2',3'-Dimethyl-biphenyl-2-yl)-propionic acidHCID 57560105—
Reactantfuran-3-carboxylic acid N'-isopropyl-hydrazideHCID 58689920—
SolventDimethylformamideHCID 6228—
ProductFuran-3-carboxylic acid N'-[3-(2',3'-dimethyl-biphenyl-2-yl)-propionyl]-N'-isopropyl-hydrazideHCID 5756012941.4%

Reaction Steps

A solution of 3-(2′,3′-dimethyl-biphenyl-2-yl)-propionic acid (227 mg, 0.89 mmoles) and furan-3-carboxylic acid N′-isopropyl-hydrazide (150 mg, 0.89 mmoles) in DMF (8 mL) was treated with triethylamine (0.37 mL, 2.67 mmoles), HOBT (144 mg, 1.07 mmoles) and EDCI (205 mg, 1.07 mmoles) at room temperature for 48 h. The reaction mixture was partitioned between 1N HCl and dichloromethane. The organic layer was washed successively with 1N NaOH and brine, then dried over sodium sulfate, filtered and concentrated. The crude was absorbed on silica and purified on a silica gel column with a 20-50% ethyl acetate/hexanes gradient to afford the product (149 mg, 41%). LC-MS m/e 405.52 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485752B2
Source datasetuspto-grants-2009_02
ORD IDord-01ddc6c9684c4daf80705b7f8393ade4
Source noteuspto-grants-2009_02