HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 59420736, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 45119426 | HCID 45119426 | — |
| Reactant | HCID 59420848 | HCID 59420848 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 59420736 | HCID 59420736 | 43% |
Reaction Steps
A suspension of Ethyl 2-(6-(5-methyl-1H-pyrazol-3-ylamino)-2-chloropyrimidin-4-yl)acetate (0.676 g, 2.29 mmol) and N-(4-mercaptophenyl)propionamide (0.415 g, 2.29 mmol) in t-butanol (10 ml) was heated under reflux overnight. Reaction mixture was then cooled to room temperature, ethyl acetate (20 ml) added causing precipitation of product. Solid was collected by filtration, washed with sat. sodium hydrogen carbonate solution, water, diethyl ether then dried by suction to leave title compound as a yellow solid (0.425 g, 43%). 1H NMR (DMSO) 1.12 (3H, t), 1.20 (3H, t), 2.00 (3H, s), 2.40 (2H, q), 3.66 (2′H, s), 4.11 (2H, q), 5.05 (1H, br s), 5.30 (1H, br s), 7.53 (2H, d), 7.79 (2H, d), 10.20 (1H, s); ES+441.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637511B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-8ea1f24bc19a42e7b8b1f2ace477c92e |
| Source note | uspto-grants-2014_01 |