HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylethylenediamine → 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (2-dimethylamino-ethyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid(3-dimethylamino-propyl)-amide | HCID 10347182 | — |
| Reactant | 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid | HCID 21899984 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (2-dimethylamino-ethyl)-amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-3ca0d79fc86c43448116278412d7d99e |
| Source note | uspto-grants-2006_11 |