HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[(1-Acetyl-2-indolyl)carbonylamino]-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 1-acetylindole-2-carboxylic Acid | HCID 10219867 | — |
| Reactant | 2-Amino-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazole | HCID 18946571 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(1-Acetyl-2-indolyl)carbonylamino]-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazole | HCID 18946565 | — |
Reaction Steps
1.5 g of 2-amino-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazole, 1 g of 1-acetylindole-2-carboxylic acid, 0.7 ml of triethylamine and 2.39 g of BOP are dissolved in 15 ml of dichloromethane. The reaction mixture is stirred overnight at room temperature and then concentrated under vacuum. The residue is taken up in ethyl acetate and the solution is successively washed with a buffer solution, pH=2, with a 5% solution of NaHCO3 and with water, and then the organic phase is dried over MgSO4 and concentrated under vacuum. The residue is purified by chromatography on a silica gel, eluent:dichloromethane/ethyl acetate 100/2.5 (v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05314889 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-31d9b796e069467f968c850c7f808add |
| Source note | uspto-grants-1994_05 |