HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 67550203, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl 4-amino-1-methyl-1H-pyrrole-2-carboxylate | HCID 2794657 | — |
| Reactant | Ethyl 5-amino-1H-indole-2-carboxylate | HCID 10726872 | — |
| Reactant | HCID 67550255 | HCID 67550255 | — |
| Product | HCID 67550203 | HCID 67550203 | 66% |
Reaction Steps
A solution of compound 2 (200 mg, 0.372 mmole) and freshly prepared of 5-aminoindole-2-carboxylic acid ethyl ester (as described above) methyl 4-amino-1-methyl-1H-pyrrole-2-carboxylate in dry DMF (5.0 ml) was kept at ambient temperature for 48 hours and evaporated. The residue was re-precipitated from DMF (1.0 ml)-0.01 M HCl (10 ml). The precipitate was collected on the filter, washed with water (3×5 ml) end ether (2×3 ml) and dried in vacuo over phosphorus pentoxide to give 142 mg (66%) of 5-({1-[2-(2-ethoxycarbonyl-1H-indol-5-ylcarbamoyl)-1H-indol-5-yl]-methanoyl}-amino)-1H-indole-2-carboxylic acid ethyl ester 21. The structure was confirmed by ES MS and 1H-NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906103B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-11cadc3b8d9744d4a029a8c99b565bce |
| Source note | uspto-grants-2005_06 |