Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 87350309 | HCID 87350309 | — |
| Reactant | HCID 87350463 | HCID 87350463 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67303576 | HCID 67303576 | — |
| Product | HCID 67308401 | HCID 67308401 | — |
Reaction Steps
Methanesulfonyl chloride (30 μL, 0.390 mmol) and triethylamine (162 μL, 1.17 mmol) were added to a solution of 1-{1,10-bis[(4-chlorophenyl)sulfonyl]-4,5,6,7,8,9-hexahydro-1H-4,8-epiminocycloocta[c]pyrazol-6-yl}-N-hydroxymethanimine and 1-{2,10-bis[(4-chlorophenyl)sulfonyl]-4,5,6,7,8,9-hexahydro-1H-4,8-epiminocycloocta[c]pyrazol-6-yl}-N-hydroxymethanimine (60) (73 mg, 0.130 mmol) in CH2Cl2 (1 mL) and the resulting solution was stirred at room temperature for 0.5 h. The reaction mixture was diluted with CH2Cl2 and washed with saturated aqueous NaHCO3. The organic phase was dried (Na2SO4), filtered, and concentrated to give 1,10-bis[(4-chlorophenyl)sulfonyl]-4,5,6,7,8,9-hexahydro-1H-4,8-epiminocycloocta[c]pyrazole-6-carbonitrile and 2,10-bis[(4-chlorophenyl)sulfonyl]-4,5,6,7,8,9-hexahydro-2H-4,8-epiminocycloocta[c]pyrazole-6-carbonitrile (61). MS (ESI) 537.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283358B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-cc36f6685e3b4f5bb1183d50b0767a1f |
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| Source note | uspto-grants-2012_10 |
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