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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719701Generated: October 30, 2026

N,N-Dimethylethylenediamine → 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (2-dimethylamino-ethyl)-amide

https://huagongshe.com/reaction/719701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid(3-dimethylamino-propyl)-amideHCID 10347182—
Reactant3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acidHCID 21899984—
SolventTetrahydrofuranHCID 8028—
Product3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (2-dimethylamino-ethyl)-amideHCID 10322522—

Reaction Steps

3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (2-dimethylamino-ethyl)-amide was synthesized as described for 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid (3-dimethylamino-propyl)-amide. 3′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (1.02 g, 2.8 mmol, 1 eq.) in anhydrous THF was treated with 1,1-carbonyldiimidazole (0.46 g, 2.86 mmol, 1.02 eq.) and N,N-dimethylethylenediamine (0.30 g, 3.36 mmol, 1.2 eq.) as described. When complete, the reaction was worked up as described leaving a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132456B2
Source datasetuspto-grants-2006_11
ORD IDord-3ca0d79fc86c43448116278412d7d99e
Source noteuspto-grants-2006_11