HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 57880864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(3,4-Dibromo-benzyl)-piperazine-1-carboxylic acid phenylamide | HCID 11648132 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57880864 | HCID 57880864 | — |
Reaction Steps
To a solution of 4-(3,4-dibromo-benzyl)-piperazine-1-carboxylic acid phenylamide (0.02 g) in DMF (0.6 mL) was added NaH (60% dispersion in oil; 3 mg) in one portion. The resulting mixture was allowed to stir for 30 min, then was treated with MeI (0.005 mL), and was stirred at rt for 12 h. The mixture was concentrated and the residue was purified by column chromatography (5% MeOH/DCM), giving the product as a white solid (0.015 g). 1H NMR (400 MHz, CDCl3): 7.54-7.50 (m, 2H), 7.33-7.31 (m, 2H), 7.12-7.05 (m, 4H), 3.34 (s, 2H), 3.22-3.20 (m, 6H), 2.23-2.21 (m, 4H), 1.63 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169224B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-7e644f4d3ce04f658496edec5027d4de |
| Source note | uspto-grants-2015_10 |