HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 66706065, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 66706189 | HCID 66706189 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66706065 | HCID 66706065 | 71.8% |
Reaction Steps
Process 3: To the dichloromethane (1 mL) solution of the crude product of 4′-{{1-[5-(3-aminopropoxy)pyrimidin-2-yl]-4-butyl-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}biphenyl-2-carbonitrile (45 mg), pyridine (9.7 mg, 0.123 mmol) and acetyl chloride (8.3 mg, 0.106 mmol) were added and stirred at room temperature overnight. The reaction mixture was added water, and extracted with ethyl acetate. The organic layer was combined, washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain N-{3-{2-{4-butyl-5-[(2′-cyanobiphenyl-4-yl)methyl]-2-methyl-6-oxopyrimidin-1 (6H)-yl}pyrimidin-5-yl oxy}propyl}acetamide (35 mg) as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664226B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-f01d5e72d87a41aa8a578e4592698979 |
| Source note | uspto-grants-2014_03 |