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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719695Generated: November 1, 2026

N,N-Dimethyl-1,3-propanediamine → 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (3-dimethylamino-propyl)-amide

https://huagongshe.com/reaction/719695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acidHCID 21899982—
SolventTetrahydrofuranHCID 8028—
Product4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (3-dimethylamino-propyl)-amideHCID 998111685.7%

Reaction Steps

Prepared in the same manner as described for example 1. A solution of 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (0.38 g, 1.04 mmol, 1 eq.) in anhydrous THF was treated with 1,1′-carbonyldiimidazole (0.17 g, 1.06 mmol, 1.02 eq.) and warmed as described. The reaction was allowed to cool and then treated with 3-(dimethylamino)propylamine (0.13 g, 1.25 mmol, 1.2 eq.). The reaction was treated as described in example 1 to give a yellow oil. The oil was purified by silica gel flash chromatography using 10% 2M NH3 in methanol in diethyl ether as the mobile phase. Fractions containing the product were pooled and the solvent removed in vacuo leaving 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (3-dimethylamino-propyl)-amide (0.40 g, 85% yield) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132456B2
Source datasetuspto-grants-2006_11
ORD IDord-6f0870eead644d15bee59f0470cb3272
Source noteuspto-grants-2006_11