HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 9928346, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-ethylpropanediamide | HCID 263023 | — |
| Reactant | HCID 11245724 | HCID 11245724 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9928346 | HCID 9928346 | — |
Reaction Steps
2-Amino-4-(1,3-benzodioxol-5-yl)-6-(phenylsulfanyl)-3,5-dicyanopyridine (5.00 g, 13.43 mmol) [preparation analogously to J. M. Quintela, J. L. Soto, Anales de Quimica 79, 368–372 (1983)] is initially charged with ethyl malonamide (4.23 g, 23.22 mmol) in absolute DMF (30 ml) under an atmosphere of argon. Potassium tert-butoxide (3.01 g, 26.85 mmol) is added, and the solution is then stirred at room temperature for 22 hours. The mixture is poured into water (300 ml). The mixture is then extracted three times with ethyl acetate (300 ml each) and the combined organic phases are dried over magnesium sulfate, filtered and concentrated to about 100 ml. The precipitated crystals are filtered off with suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129255B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-3358086eb5d543968b9a9722a51cbf6c |
| Source note | uspto-grants-2006_10 |