HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dimethylethylenediamine → 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid(2-dimethylamino-ethyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid | HCID 21899992 | — |
| Product | 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid(2-dimethylamino-ethyl)-amide | HCID 10029777 | 94% |
Reaction Steps
Prepared in the same manner as described for example 1. A solution of 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid(0.68 g, 1.87 mmol, 1 eq.) was treated with 1,1′-carbonyldiimidazole (0.31 g, 1.91 mmol, 1.02 eq.) and warmed as described. The reaction was allowed to cool and then treated with N′,N-dimethylethylenediamine (0.20 g, 2.24 mmol, 1.2 eq.). The reaction was treated as described in example 1 to give 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid(2-dimethylamino-ethyl)-amide (0.76 g, 94% yield) as a faint yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-739f519caed545349b042b959e095a2b |
| Source note | uspto-grants-2006_11 |