HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21552248, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21552259 | HCID 21552259 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 21552248 | HCID 21552248 | — |
Reaction Steps
If the 3-(2'-methyl-2'-nitrobutyl)-5-methoxy-indole obtained as intermediate product in Example 2 is methylated by the procedure described in Example 4 (or by means of sodium hydride and methyl iodide in hexamethyl phosphoric acid triamide), 1-methyl-3-(2'-methyl-2'-nitrobutyl)-5-methoxy-indole is obtained and melts at 95°-96°C. after crystallisation from acetone/water and distillation. Catalytic reduction thereof yields 1-methyl-3-(2'-methyl-2'-aminobutyl)-5-methoxy-indole. Melting point of the benzoic acid salt 179.5°-184°C. (insoluble in ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947584 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-8fb34a85a61c4c2781aa6f678718e8bf |
| Source note | uspto-grants-1976_03 |