Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 4-(3,4-Dichloro-phenoxy)-[1,4']bipiperidine | HCID 22397434 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86595132 | HCID 86595132 | — |
Reaction Steps
tert-Butanol (0.48 ml) in dichloromethane (2 ml) was added to a solution of chlorosulfonylisocyanate (0.43 ml) in dichloromethane (5 ml) stirring at 0° C. The resulting solution was then added to a solution of 4-(3,4-dichlorophenoxy)-1,4′-bipiperidine (1.6 g) and triethylamine (0.77 ml) in dichloromethane (20 ml) at 0° C. After stirring at 0° C. for 2 h, the reaction mixture was washed with 0.1M hydrochloric acid (30 ml), dried (MgSO4) and evaporated. The residue was triturated with diethylether (20 ml) to give the title compound as a white solid. (1.9 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07307090B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-0e9ebc0b8b87447681b9bb90eaebebea |
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| Source note | uspto-grants-2007_12 |
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