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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724156Generated: November 3, 2026

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

https://huagongshe.com/reaction/1724156

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—
Reactantthiophene-3-carboxylic acid N'-isopropyl-hydrazideHCID 59642162—
SolventDimethylformamideHCID 6228—
ProductThiophene-3-carboxylic acid N'-[3-(2',3'-dimethyl-biphenyl-2-yl)-propionyl]-N'-isopropyl-hydrazideHCID 5756012150.5%

Reaction Steps

A solution of 3-(2′,3′-dimethyl-biphenyl-2-yl)-propionic acid (207 mg, 0.81 mmoles) and thiophene-3-carboxylic acid N′-isopropyl-hydrazide (150 mg, 0.81 mmoles) in DMF (8 mL) was treated with triethylamine (0.34 mL, 2.44 mmoles), HOBT (132 mg, 0.98 mmoles) and EDCI (156 mg, 0.98 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 (172 mg, 50%). LC-MS m/e 421.46 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485752B2
Source datasetuspto-grants-2009_02
ORD IDord-fd849881b6594c7d86ebba7e1167f7f6
Source noteuspto-grants-2009_02