HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → {4-[4-(5-methoxy-1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | {4-[4-(5-methoxy-1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine | HCID 10029113 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | {4-[4-(5-methoxy-1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine dihydrochloride | HCID 10029112 | — |
Reaction Steps
To prepare the dihydrochloride the polar diastereoisomer of {4-[4-(5-methoxy-1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine (170 mg, 0.4 mmole) was dissolved in ethyl methyl ketone (5 ml) and chlorotrimethylsilane (125 μl, 1.0 mmole) was added. The solid thereby formed was filtered off and dried. The polar {4-[4-(5-methoxy-1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine dihydrochloride was thereby obtained as a colourless solid with an m.p. of 201°-203° C. in a yield of 200 mg (Example 8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759385B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-ba6d2c0f71c84f17bd2bdecc1785a5c4 |
| Source note | uspto-grants-2010_07 |