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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719715Generated: October 31, 2026

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

https://huagongshe.com/reaction/719715

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-4-carboxylic acidHCID 21899979—
SolventTetrahydrofuranHCID 8028—
Product3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid (4-dimethylamino-butyl)-amideHCID 10482743—

Reaction Steps

3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-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-4-carboxylic acid (1.50 g, 4.12 mmol, 1 eq.) in anhydrous THF was treated with 1,1-carbonyldiimidazole (0.68 g, 4.20 mmol, 1.02 eq.) and 4-dimethylaminobutylamine (0.57 g, 4.94 mmol, 1.2 eq.). 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-fa4c5514457b4629817b57e1f08fad89
Source noteuspto-grants-2006_11