HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 58303957, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 66927142 | HCID 66927142 | — |
| Product | HCID 58303957 | HCID 58303957 | — |
Reaction Steps
To the solution of 9-1 (prepared according to the same procedure of ethyl 2-(5-bromo-7-fluoro-4-methoxy-1H-indol-3-yl)acetate) (2.0 g, 6.3 mmol) in anhydrous DMF (15 mL) was added KOH (1.12 g, 20 mmol), and iodomethane (1.8 g, 12.7 mmol). The mixture was stirred for 1 h at room temperature. After quenching with water, the reaction mixture was extracted with ethyl acetate (150 mL×3). The combined organic layers were dried over anhydrous sodium sulfate. After filtration and concentration, a residue 9-2 (3.0 g, crude) was obtained as yellow oil which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912220B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-b8122d7359814306bcf66bbbde4f1426 |
| Source note | uspto-grants-2014_12 |