HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium hydride → 4-Chloro-6-(2,6-difluoro-phenylamino)-2-methylsulfanyl-pyrimidine-5-carbonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2,6-Difluoroaniline | HCID 79647 | — |
| Edukt | 4,6-Dichloro-2-(methylsulfanyl)pyrimidine-5-carbonitrile | HCID 4201620 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-Chloro-6-(2,6-difluoro-phenylamino)-2-methylsulfanyl-pyrimidine-5-carbonitrile | HCID 21114472 | 87% |
Reaktionsschritte
2,6-di-Fluoroaniline (2.66 mL, 24 mmol), DMSO (12 mL) and NaH (0.912 g, 22.8 mmol) were combined at 23°. When the foaming ceased 4,6-Dichloro-2-methylsulfanyl-pyrimidine-5-carbonitrile [Santilli, et al., J. Heterocycl. Chem. 1971, 8, 445-453] (5.0 g, 22.82 mmol) was added in DMSO (12 mL). The reaction exothermed and the temperature was moderated with cold H2O bath, then stirred at 23° for 3 h. The reaction was diluted with EtOAc (300 mL) and washed with H2O (4×) and satd aq NaCl (1×). Dried (Na2SO4) and concentrated to afford 6.21 g (82%) of a tan foam. LC MS m/z=313 (MH+), Rt=2.37 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07700768B2 |
| Quelldatensatz | uspto-grants-2010_04 |
| ORD ID | ord-d2c8cdebd00f4ca4997ef5cbe62ac2fb |
| Quellennotiz | uspto-grants-2010_04 |