HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 16665204, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 28749130 | HCID 28749130 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 16665204 | HCID 16665204 | 44% |
Reaction Steps
A mixture of N-phenyl-4-piperazin-1-yl-benzamide (4 mg, 0.02 mmol), methyl α-bromophenyl acetate (3 μL, 0.02 mmol), and K2CO3 (3 mg, 0.02 mmol) in DMF (1 mL) was stirred for 16 h. The mixture was diluted with H2O and extracted with methanolic DCM (2×). The combined organic layers were dried (MgSO4) and concentrated to give an oil, which was purified by PTLC to give a white solid (3 mg, 44%). MS (ESI): mass calcd. for C26H27N3O3, 429.51. m/z found, 430.4 [M+H]+. 1H NMR (CDCl3): 7.71 (d, J=8.9, 2H), 7.69 (br s, 1H), 7.61 (d, J=7.6, 2H), 7.47-7.45 (m, 2H), 7.39-7.33 (m, 5H), 7.12 (t, J=7.4, 1H), 6.89 (d, J=8.9, 2H), 4.07 (s, 1H), 3.71 (s, 3H), 3.36-3.33 (m, 4H), 2.64-2.61 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183239B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-be5b1afcc50a46f395323b912d3c032c |
| Source note | uspto-grants-2012_05 |