HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 58064922, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66681528 | HCID 66681528 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58064922 | HCID 58064922 | — |
Reaction Steps
To a suspension of benzamide N-(4-(biphenyl-4-yl)-6,7-dimethoxynaphthalen-1-yl)5-bromobenzo[1,3]dioxole-4-carboxamide (1 mmol), and NaH (3 mmol) in dry DMF (20 mL) was added MeI (2 equiv). The reaction mixture was stirred over night, diluted with ether and then washed with 10% HCl and brine. The residue was subjected to column chromatography on silica using 2% methanol in chloroform to provide product N-(4-(biphenyl-4-yl)-6,7-dimethoxynaphthalen-1-yl)5-bromo-N-methylbenzo[1,3]dioxole-4-carboxamide as an off white solid. 1H NMR (400 MHz) (CDCl3) δ 3.39-3.60 (m, 3H, N—CH3), 3.66-3.80 (m, 3H, O—CH3), 3.96-4.00 (m, 3H, O—CH3), 5.03-6.18 (m, 2H, O—CH2O), 6.30-7.69 (m, 15H, aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741917B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-606aeaf5452c42b38e5450389fb256e4 |
| Source note | uspto-grants-2014_06 |