HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[(2-Indolyl)carbonylamino]-5-methoxy-4-phenylthiazole
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-5-methoxy-4-phenylthiazole | HCID 18946566 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(2-Indolyl)carbonylamino]-5-methoxy-4-phenylthiazole | HCID 18946577 | — |
Reaction Steps
3.15 g of 2-amino-5-methoxy-4-phenylthiazole are dissolved in 60 ml of CH2Cl2. 3.26 g of 1-acetylindole-2-carboxylic acid, 8.12 g of BOP and 1.86 g of triethylamine are added, and the reaction mixture is stirred at room temperature for one week. 50 ml of water are added and the organic phase is decanted, dried over Na2SO4, filtered and concentrated under vacuum. The residue is taken up in 100 ml of methanol, and 10 g of K2CO3 are added and the mixture is stirred overnight at room temperature. The mixture is concentrated under vacuum, and the residue is taken up in water, and the precipitate formed is separated by filtration and washed with CH2Cl2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380736 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-e12a4fe56acd4f7cba2026109b320220 |
| Source note | uspto-grants-1995_01 |