HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 24748349, compound → HCID 16110666, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 24748349 | HCID 24748349 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16110666 | HCID 16110666 | 90% |
Reaction Steps
The title compound was prepared from 1-(5-(2,6-dimethoxypyrimidin-4-yl)oxazol-2-yl)-7-phenylheptan-1-one (20 mg, 0.051 mmol) following General Procedure H. Flash chromatography (EtOAc) yielded the title compound as a white solid (16 mg, 90%): 1H NMR (CDCl3/CD3OD, 500 MHz) δ 7.92 (s, 1H), 7.28-7.24 (m, 2H), 7.18-7.15 (m, 3H), 6.19 (s, 1H), 3.06 (t, 2H, J=7.4 Hz), 2.58 (t, 2H, J=7.7 Hz), 1.73 (quintet, 2H, J=7.3 Hz), 1.61 (quintet, 2H, J=7.4 Hz), 1.38-1.36 (m, 4H); 13C NMR (CDCl3, 125 MHz) δ 188.3, 163.8, 158.0, 151.7, 144.9, 142.5, 139.1, 129.8, 128.3, 128.1, 125.5, 98.8, 39.2, 35.7, 31.1, 28.81, 28.78, 23.5; MALDI-FTMS m/z 368.1595 (M+H+, C20H22N3O4, requires 368.1605).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915270B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-68732565c39649399dbc1a18ee5a43b1 |
| Source note | uspto-grants-2011_03 |