HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 2-Iodo-5-methyl-4-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 4-Nitro-m-toluidine | HCID 11898 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Product | 2-Iodo-5-methyl-4-nitroaniline | HCID 58121243 | — |
Reaction Steps
3-Methyl-4-nitroaniline was treated with iodine and silver sulfate to give 2-iodo-5-methyl-4-nitroaniline. Treatment of the nitroaniline with 2-(trimethylsilyl)acetylene under the typical Sonogashira conditions gave 5-methyl-4-nitro-2-[(trimethylsilyl)ethynyl]aniline, which was treated with a base in an aqueous methanolic solution to give 2-ethynyl-5-methyl-4-nitroaniline. A subsequent base-induced cyclization at an elevated temperature gave 5-nitro-6-methylindole, which was treated under a high pressure hydrogenation condition to provide 5-amino-6-methylindole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781591B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-187d4a186cf84ac596d6a843501fc9bd |
| Source note | uspto-grants-2010_08 |