HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-4-methylpyrimidine → 2-Propen-1-yl {3-[(2-chloro-4-pyrimidinyl)acetyl]phenyl}carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-4-methylpyrimidine | HCID 11629607 | — |
| Reactant | Ethyl 3-{[(2-propen-1-yloxy)carbonyl]amino}benzoate | HCID 57989833 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Product | 2-Propen-1-yl {3-[(2-chloro-4-pyrimidinyl)acetyl]phenyl}carbamate | HCID 57989981 | 51.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Ethyl 3-{[(2-propen-1-yloxy)carbonyl]amino}benzoate (20.0 g, 80.24 mmol) was dissolved in 1 M LiHMDS in THF (260 mL) and cooled to 0° C. A solution containing 2-chloro-4-methylpyrimidine (10.32 g, 80.24 mmol) in 20 mL dry THF was added to the reaction mixture. The reaction was stirred at 0° C. for 2 h, quenched with MeOH (100 mL), dried directly onto silica, and purified via flash chromatography EtOAc/CH2Cl2 0-100% gradient run over 60 min. The desired fractions were combined and the solvent was removed to give the title compound (13.6 g, 51% yield); ES-LCMS m/z 332 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642759B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-236d756f44f147668b4d5ed6338fc3b1 |
| Source note | uspto-grants-2014_02 |