HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → {4-[3-(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-[3-(1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine | HCID 57438232 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | {4-[3-(1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine dihydrochloride | HCID 67532584 | — |
Reaction Steps
To prepare the dihydrochloride the non-polar diastereoisomer of {4-[3-(1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine (208 mg, 0.52 mmole) was dissolved in ethyl methyl ketone (5 ml) and chlorotrimethylsilane (165 μl, 1.3 mmole) was added. The solid thereby obtained was filtered off and dried. The non-polar {4-[3-(1H-indol-3-yl)piperidine-1-yl]-1-phenylcyclohexyl}-dimethylamine dihydrochloride was thereby obtained as a colourless solid with an m.p. of 188°-190° C. in a yield of 245 mg (100%) (Example 9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759385B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-515b6b68c437472289eda9bf7ccf8f49 |
| Source note | uspto-grants-2010_07 |