Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719703Generated: October 31, 2026

4-Dimethylaminobutylamine → 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (4-dimethylamino-butyl)-amide

https://huagongshe.com/reaction/719703

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-DimethylaminobutylamineHCID 77063—
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 (4-dimethylamino-butyl)-amideHCID 10322129—

Reaction Steps

3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (4-dimethylamino-butyl)-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 (0.95 g, 2.61 mmol, 1 eq.) in anhydrous THF was treated with 1,1-carbonyldiimidazole (0.43 g, 2.66 mmol, 1.02 eq.) and 4-dimethylaminobutylamine (0.36 g, 3.13 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-f8a2ef9a435b42beb45888a355367f9c
Source noteuspto-grants-2006_11