HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-(4-[5,6-Dimethoxy-1,2-benzisoxazol-3-yl]piperidyl}-2-methyl indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5,6-Dimethoxy-3-(4-piperidyl)-1,2-benzisoxazole | HCID 13076426 | — |
| Reactant | 2-Methyl-3-(phenylsulfonylpropyl)indole | HCID 13450900 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-[5,6-Dimethoxy-1,2-benzisoxazol-3-yl]piperidyl}-2-methyl indole | HCID 86738587 | 26.8% |
Reaction Steps
A stirred mixture of 5.0 g of 5,6-dimethoxy-3-(4-piperidyl)-1,2-benzisoxazole, 6.78 g of 2-methyl-3-(phenylsulfonylpropyl)indole, 120 ml of dimethylformamide and 15.0 g of anhydrous potassium carbonate was heated to 90° for 6 hrs and overnight at ambient temperature. The mixture was poured into water (300 ml) and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield a solid. The solid was purified by passing it through a silica gel column (20:1) and eluting it with dichloromethane-methanol (1%). Recrystallization two times from ethanol-water yielded 2.0 g (24%) of product, mp 176°-178°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352811 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-11c789af77164c3e95c1fe0087bc6bf8 |
| Source note | uspto-grants-1982_10 |