HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → HCID 13179835, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13179834 | HCID 13179834 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13179835 | HCID 13179835 | — |
Reaction Steps
2.5 ml of acetic acid and then 1.4 ml of an aqueous 40% formaldehyde solution were slowly added with stirring at 0° to 5° C. under an inert atmosphere to 2.5 ml of an aqueous 35% dimethylamine solution and then a solution of 5.5 g of 4-(1-benzyl-piperidin-3-yl)-1H-indole in 25 ml of acetic acid was added to the mixture. The mixture was stirred at room temperature for 90 minutes and was then diluted with water. Sodium hydroxide was added to the mixture to make it basic and the mixture was filtered. The recovered product was washed with water, dried under reduced pressure and crystallized from benzene to obtain 3 g of N,N-dimethyl-4-(1-benzyl-piperidin-3-yl)-1H-indole-3-methanamine melting at ≃150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04447438 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-b72d16f19c834caa8bade6fa193f4455 |
| Source note | uspto-grants-1984_05 |