HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N,N-Dimethyl-1-(2,3,4,9-tetrahydrothiopyrano[2,3-b]indol-4-yl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-(2,3,4,9-Tetrahydrothiopyrano[2,3-b]indol-4-yl)methanamine | HCID 3056088 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Product | N,N-Dimethyl-1-(2,3,4,9-tetrahydrothiopyrano[2,3-b]indol-4-yl)methanamine | HCID 3056094 | 66% |
Reaction Steps
To a solution of 4-aminomethyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole (1.8 g) in tetrahydrofuran (80 ml) are added acetic acid (2.3 ml), 37% formalin (5.6 ml) and sodium cyanoborohydride (1.35 g) successively. The mixture is stirred at room temperature for 1 hour and evaporated to remove the solvent. The residue is extracted with ether after addition of some pieces of ice and an 10% aqueous solution of sodium hydroxide. The extract is washed with water, dried and evaporated to give an oil (3 g). The oil is chromatographed on a column of basic alumina (70 g) and eluted with ethyl acetate-hexane (1:1). The eluate is evaporated to give crystals of the title compound (1.34 g) melting at 121°-122° C. Yield: 66%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256640 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-9fbfb24f88004a528058fc4d373d827d |
| Source note | uspto-grants-1981_03 |