HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21249511, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-Indole-2-carboxylic acid, 1-methyl- | HCID 27695 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 2-Amino-4-(4-methoxyphenyl)thiazole | HCID 159644 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21249511 | HCID 21249511 | — |
Reaction Steps
1 g of 2-amino-4-(4-methoxyphenyl)thiazole is dissolved in 20 ml of dimethylformamide and, successively, 0.6 g of 1-methylindole-2-carboxylic acid, then 1.6 g of 1-benzotriazolyl-oxytris(dimethylamino)phosphonium hexafluorophosphate (BOP) and then 0.7 g of triethylamine are added to the reaction mixture at ambient temperature. The reaction mixture is left at ambient temperature for about 12 hours, while stirring well, before pouring into 100 ml of ice-water; the aqueous phase obtained is then extracted with twice 50 ml of ethyl acetate. The organic extracts are dried over anhydrous magnesium sulphate and evaporated to dryness. The residual solid is purified by chromatography on a silica column (eluant: CH2Cl2). Yield
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05189049 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-a8f746cf51124fb59b56d62f31b823ff |
| Source note | uspto-grants-1993_02 |