HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Methyl-1H-indol-5-amine → 5-(3,4-dimethoxyphenyl)-4-(7-methyl-1H-indol-5-ylamino)nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Methyl-1H-indol-5-amine | HCID 15434501 | — |
| Reactant | 5-(3-bromophenyl)-4-(1H-indol-5-ylamino)nicotinonitrile | HCID 24866681 | — |
| Reactant | 4-Chloro-5-(3,4-dimethoxyphenyl)nicotinonitrile | HCID 25129785 | — |
| Product | 5-(3,4-dimethoxyphenyl)-4-(7-methyl-1H-indol-5-ylamino)nicotinonitrile | HCID 44573900 | — |
Reaction Steps
Following procedures analogous to those described for preparing compound 113 (Example 2, Method B), the title compound was prepared from 4-chloro-5-(3,4-dimethoxyphenyl)nicotinonitrile and 5-amino-7-methylindole. MS: 385.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781591B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-34a78f18d3634db19cda05bfc27ded4f |
| Source note | uspto-grants-2010_08 |