HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-1H-indole-3-ethylamine monohydrochloride → N-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-(phenylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-1H-indole-3-ethylamine monohydrochloride | HCID 2827494 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-Anilinobenzoic acid | HCID 12850341 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-(phenylamino)benzamide | HCID 71451287 | 25.4% |
Reaction Steps
A mixture of 3-(phenylamino)benzoic acid (0.155 g, 0.727 mmol), 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.168 g; 0.727 mmol), HATU (0.303 g; 0.799 mmol) and N,N-diisopropylethyldiamine (0.313 mL; 1.82 mmol) in DMF (5 mL), was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and sodium hydrogen sulphate, the organic layer was washed with sodium carbonate, brine, dried and concentrated in vacuo. The crude mixture was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.072 g (25%) of the title compound as a pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266832B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-5d68241c1e794885b7e49bb11d5b0282 |
| Source note | uspto-grants-2016_02 |