HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-Cyano-N-(1H-indol-1-yl)-4-pyrimidinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Aminoindole | HCID 643221 | — |
| Reactant | 4-Chloropyrimidine-5-carbonitrile | HCID 13126909 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Cyano-N-(1H-indol-1-yl)-4-pyrimidinamine | HCID 15158252 | — |
Reaction Steps
To 100 ml absolute ethanol, was added 5.0 g of 1H-indol-1-amine, 5.0 g of 4-chloro-5-cyanopyrimidine and 5 ml of triethylamine. After stirring at ambient temperature for 20 hours, the mixture was poured into 400 ml water, stirred for five minutes, then extracted with ethyl acetate. The organic layer was washed with water, then dried (saturated NaCl, anhydrous MgSO4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983608 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-e13453b879254b4cb17d43532bcf19a5 |
| Source note | uspto-grants-1991_01 |