HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiopheneacetic acid → 4-(2-Ethyl-cyclohexylamino)-3-(2-thiophen-2-yl-acetylamino)-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 3-Amino-4-(2-ethyl-cyclohexylamino)-benzoic acid methyl ester | HCID 61468035 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Ethyl-cyclohexylamino)-3-(2-thiophen-2-yl-acetylamino)-benzoic acid methyl ester | HCID 86714456 | 101% |
Reaction Steps
To a solution of 0.24 g of thiophen-2-yl-acetic acid in 40 ml of dry DMF 0.11 g of HOAT, 0.36 g of EDC and 0.5 ml of DIPEA were added at 0° C. After 30 min 0.41 g of 3-Amino-4-(2-ethyl-cyclohexylamino)-benzoic acid methyl ester were added, followed by the addition of 0.5 ml of DIPEA and the reaction was stirred at rt for 48 h. The reaction was then poured into water and extracted with ethyl acetate three times. The combined organic phases were washed with saturated aqueous sodium bicarbonate solution and brine, dried over magnesium sulphate and concentrated to obtain 0.60 g (97%) of 4-(2-Ethyl-cyclohexylamino)-3-(2-thiophen-2-yl-acetylamino)-benzoic acid methyl ester, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156796B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-7e9aff7c81b24f5e95761f7d59b77151 |
| Source note | uspto-grants-2015_10 |