Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | HCID 69204374 | HCID 69204374 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 86596304 | HCID 86596304 | — |
Reaction Steps
Sodium hydride (60% dispersion, 0.30 g, 0.75 mmol) was added to a solution of 2,4-dichloropyrimidine (0.75 g, 0.50 mmol) and (4-methoxyphenyl)-carbamic acid pyridin-3-ylmethyl ester (1.3 g, 0.50 mmol) in DMF (5 mL). The mixture was allowed to stir at room temperature for 2 h. The resulting solution was diluted with sat. aqueous ammonium chloride and ethyl acetate. The organic phase was separated and washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated to afford a colorless oil. This oil was purified via column chromatography on silica gel (gradient elution with 0-5% methanol-dichloro-methane) to afford (2-chloropyrimidin-4-yl)-(4-methoxyphenyl)carbamic acid pyridin-3-ylmethyl ester as a tan solid. MS (MH+) 371; Calculated 370.8 for C18H15ClN4O3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07442698B2 |
|---|
| Source dataset | uspto-grants-2008_10 |
|---|
| ORD ID | ord-1068acab4de246d79cbf3963a768534c |
|---|
| Source note | uspto-grants-2008_10 |
|---|