HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 21106603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-[4-(4-Bromo-1-oxo-1H-phthalazin-2-yl)-phenyl]acetamide | HCID 21106602 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21106603 | HCID 21106603 | 14% |
Reaction Steps
NaH (95%, 0.005 g, 0.21 mmol) was added slowly at RT to a solution of N-[4-(4-Bromo-1-oxo-1H-phthalazin-2-yl)-phenyl]acetamide (0.070 g, 0.20 mmol) in DMF (2 ml). Stirring was continued for 1 h before ethyl iodide (0.046 g, 0.29 mmol) was added. Stirring was continued for 12 h before the solvent was evaporated in vacuum. The resulting raw product was purified by chromatography over silica gel with heptane:EtOAc (3:1 up to 1:1) to give the title compound (0.010 g, 14% yield). MS (ESI+)=388.22 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501410B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-78c2137e25964d63bff8a2c9337b58ec |
| Source note | uspto-grants-2009_03 |