HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 58458903, compound → HCID 136163962, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 58458903 | HCID 58458903 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 136163962 | HCID 136163962 | 97% |
Reaction Steps
A yellow solution of 5-(benzyloxy)-2-ethoxy-6-(3-(4-fluorobenzyl)-1,2,4-oxadiazol-5-yl)-3-methylpyrimidin-4(3H)-one (0.150 g, 0.3421 mmol) in TFA (5 mL) was stirred 6 h at room temperature. Then, the reaction mixture was concentrated and the resulting yellow solid was heated with 1:1 EtOH/H2O and filtered to afford the title compound (0.11 g, 97%) as pale yellow solid. 1HNMR (500 MHz, CDCl3) δ: 9.49 (1H, s), 7.30 (2H, dd, J=8.4, 5.4 Hz), 7.02 (2H, t, J=8.6 Hz), 4.52 (2H, q, J=7.0 Hz), 4.15 (2H, s), 3.49 (3H, s), 1.44 (3H, t, J=7.0 Hz). HRMS (M+H) calcd for C16H16N4O4F: 347.1156. found: 347.3845. Anal calcd for C16H15N4O4F: C, 55.49; H, 4.36; N, 16.17; F, 5.48. found: C, 55.14; H, 4.32; N, 15.66; F, 5.85.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383639B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-9135babb5c564e67b1ecd49224f7e94f |
| Source note | uspto-grants-2013_02 |