HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 16110608, compound → HCID 16110640, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 16110608 | HCID 16110608 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16110640 | HCID 16110640 | 27% |
Reaction Steps
The title compound was prepared from 3-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)phenol (29 mg, 0.062 mmol) following General Procedure D. Preparative thin layer chromatography (30% EtOAc) yielded the title compound as a white solid (5.2 mg, 27%): 1H NMR (CD3OD, 500 MHz) δ 7.74 (s, 1H), 7.38-7.37 (m, 2H), 7.32-7.29 (m, 3H), 7.24-7.23 (m, 2H), 7.21-7.20 (m, 1H), 6.95-6.94 (m, 1H), 3.14 (t, 2H, J=7.0 Hz), 2.69 (t, 2H, J=7.5 Hz), 1.85-1.79 (m, 2H), 1.75-1.69 (m, 2H), 1.54-1.42 (m, 4H); 13C NMR (CD3OD, 125 MHz) δ 188.5, 158.4, 157.4, 154.7, 142.9, 130.5, 128.4, 128.2, 128.2, 125.6, 123.9, 117.2, 116.5, 111.7, 38.7, 35.8, 31.5, 29.0, 29.0, 23.9; MALDI-FTMS m/z 350.1752 (M+H+, C22H24NO3, requires 350.1751).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915270B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-98d1bc089c184e4fa290f8933007cd8a |
| Source note | uspto-grants-2011_03 |