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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719714Generated: November 2, 2026

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

https://huagongshe.com/reaction/719714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
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)-bipheny-4-carboxylic acid (3-dimethylamino-propyl)-amideHCID 10075921—

Reaction Steps

3′-(2-Phenoxy-ethylsulfanylmethyl)-bipheny-4-carboxylic acid (3-dimethylamino-propyl)-amide was synthesized as described for 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid (3-dimethylamino-propyl)-amide. 3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4carboxylic acid (0.80 g, 2.19 mmol, 1 eq.) in anhydrous THF was treated with 1,1-carbonyldiimidazole (0.36 g, 2.23 mmol, 1.02 eq.) and 3-(dimethylamino)propylamine (0.27 g, 2.63 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-dc615fd2f2fb40d3984cd9ff5e877304
Source noteuspto-grants-2006_11