Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59536731 | HCID 59536731 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68646379 | HCID 68646379 | — |
Reaction Steps
Of the compound from Example 172A, 242 mg (0.86 mmol) were introduced in 12 ml of acetonitrile under argon, and admixed dropwise at −15° C. with 105 μl (1.20 mmol) of chlorosulphonyl isocyanate. The reaction mixture was stirred at −10° C. for 30 minutes. Then 12 ml of water were added and the mixture was stirred at 60° C. overnight. The reaction mixture was cooled, rendered basic using saturated aqueous sodium hydrogen carbonate solution and extracted with three times 10 ml of ethyl acetate. The organic phases were combined, dried over magnesium sulphate, filtered and freed from the solvent on a rotary evaporator. The residue was admixed with 6 ml of a 4M solution of hydrogen chloride in dioxane, the components were stirred together for 10 minutes, and the mixture was concentrated on a rotary evaporator. The residue was dried in an HV. This gave 186 mg (83% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202895B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-f82420dd3e0a4e54b904f3019166fcef |
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| Source note | uspto-grants-2012_06 |
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