Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 9961224 | HCID 9961224 | — |
| Reactant | N-Methylsulfamoyl chloride | HCID 11789235 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 70100273 | HCID 70100273 | — |
Reaction Steps
Disolve the product of Example 9 (1 equivalent) in an inert anhydrous solvent such as CH3CN, benzene or toluene and add Et3N (2 equivalents). Cool the solution to 0° C. and add N-methylsulfamoyl chloride (1.2 equivalents) [prepared as described in: J. A. Kloek and K. L. Leschinsky, J. Org. Chem., 41 (25) (1976), p. 4028-4029]. Stir the mixture at 0° C. to 25° C. for 3 h, extract, filter and evaporate to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958890 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-0858a55e8c294fcd8811637ddf713f0a |
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| Source note | uspto-grants-1999_09 |
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