HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminoindole → N5-(1H-Indol-4-yl)-N2-(2-methyl-benzofuran-7-yl)-quinoline-2,5-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminoindole | HCID 583431 | — |
| Reactant | 2-Methyl-benzofuran-7-ylamine | HCID 3157485 | — |
| Reactant | 2-Chloro-5-iodoquinoline | HCID 45789424 | — |
| Product | N5-(1H-Indol-4-yl)-N2-(2-methyl-benzofuran-7-yl)-quinoline-2,5-diamine | HCID 24990109 | — |
Reaction Steps
The title compound, MS: m/e=405.4 (M+H+), was prepared in accordance with the general method of example 1 from 5-iodo-2-chloroquinoline, (2-methyl-1-benzofuran-7-yl)amine and 4-aminoindole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825253B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-1ea50b68c6fd4579864bbaa5bf45452c |
| Source note | uspto-grants-2010_11 |