HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-methyl-1H-indol-5-amine → 5-iodo-4-[(4-methyl-1H-indol-5-yl)amino]nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-methyl-1H-indol-5-amine | HCID 15434496 | — |
| Reactant | 4-Chloro-5-iodonicotinonitrile | HCID 59431159 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Sulfate | HCID 24436 | — |
| Product | 5-iodo-4-[(4-methyl-1H-indol-5-yl)amino]nicotinonitrile | HCID 68443831 | 75% |
Reaction Steps
A mixture of 4-chloro-5-iodonicotinonitrile (5.0 g, 18.9 mmol) and 5-amino-4-methylindole (3.0 g, 20.8 mmol) in EtOH (100 mL) was heated at reflux for 3 days, cooled to r.t. and diluted with saturated aq. Na2SO4 (300 mL). The precipitated solids were collected by filtration, washed with water and dried to give 5.3 g (75%) of 5-iodo-4-[(4-methyl-1H-indol-5-yl)amino]nicotinonitrile as a grey solid. Melting range: 192-194° C.; MS (M+H+): 375.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781591B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-69d704865e544c8892253cab414e6d75 |
| Source note | uspto-grants-2010_08 |