HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 24748380, compound → HCID 16110723, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 24748380 | HCID 24748380 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16110723 | HCID 16110723 | 71.6% |
Reaction Steps
The title compound was prepared from 1-(5-(2,4-dimethoxypyrimidin-5-yl)oxazol-2-yl)-7-phenylheptan-1-one (15 mg, 0.038 mmol) following General Procedure H. Flash chromatography (EtOAc) yielded the title compound as a white solid (10 mg, 71%): 1H NMR (CDCl3, 400 MHz) δ 7.90 (s, 1H), 7.71 (s, 1H), 7.28-7.24 (m, 2H), 7.18-7.14 (m, 3H), 2.99 (t, J=7.5 Hz), 2.52 (t, 2H, J=7.8 Hz), 1.67 (quint, 2H, J=7.3 Hz), 1.55 (quint, 2H, J=7.4 Hz), 1.33-1.31 (m, 4H); 13C NMR (CDCl3, 100 MHz) δ 188.8, 160.9, 155.4, 150.6, 147.4, 142.5, 139.0, 128.2, 128.0, 126.0, 125.4, 102.6, 38.6, 35.6, 31.1, 28.8, 28.8, 23.8; MALDI-FTMS m/z 368.1613 (M+H+, C20H21N3O4, requires 368.1610).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915270B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-92bd6e059ccd4f06b0ef5326731de621 |
| Source note | uspto-grants-2011_03 |