HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → N-benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-chloroethyl)-1-methyl-4,5,6,7-tetrahydro-1H-indole | HCID 69079129 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine | HCID 17751624 | 28% |
Reaction Steps
A mixture of 4-(2-chloroethyl)-1-methyl-4,5,6,7-tetrahydro-1H-indole (0.1 g, 0.5 mmol), N-methyl-N-benzylamine (0.07 g, 0.5 mmol), K2CO3 (0.20 g, 1.45 mmol) and a catalytic amount of NaI in DMF (5 mL) is heated to 110° C. overnight. The solvent is removed at reduced pressure, diethyl ether is added to the residue and washed with water. The organic phase is dried and evaporated at reduced pressure and the resulting crude is purified by column chromatography, giving N-benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine (0.04 g, 0.14 mmol, 28%, oil). (ESI-MS m/z 283 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481567B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-cb149c94882848bd882c1aa86324c406 |
| Source note | uspto-grants-2013_07 |