HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 16110644, compound → HCID 16110704, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 16110644 | HCID 16110644 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16110704 | HCID 16110704 | 83% |
Reaction Steps
The title compound was prepared from methyl 4-(2-(7-phenylheptanoyl)oxazol-5-yl)benzoate (10 mg, 0.026 mmol) following General Procedure E. Preparative thin layer chromatography (EtOAc) yielded the title compound as a white solid (8 mg, 83%): 1H NMR (THF-d8, 500 MHz) δ 8.21 (d, 2H, J=8.5 Hz), 8.00 (d, 2H, J=8.5 Hz), 7.90 (s, 1H), 7.32-7.18 (m, 5H), 3.15 (t, 2H, J=7.5 Hz), 2.70 (t, 2H, J=7.5 Hz), 1.80-1.71 (m, 2H), 1.52-1.50 (m, 2H), 1.44-1.38 (m, 4H); 13C NMR (THF-d8, 500 MHz) δ 187.3, 165.4, 158.2, 153.2, 142.9, 132.2, 131.1, 130.7, 128.5, 128.4, 126.9, 125.7, 125.1, 38.9, 36.1, 31.6, 31.6, 29.4, 24.1; MALDI-FTMS m/z 378.1697 (M+H+, C23H24NO4, requires 378.1700).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915270B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-0f233c32272b43e0bac317a2813c9ef3 |
| Source note | uspto-grants-2011_03 |