Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59554587 | HCID 59554587 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86601407 | HCID 86601407 | — |
Reaction Steps
253 mg of compound 14b and 225 μl triethylamine were dissolved in 10 ml dichloromethane and cooled to −50° C. 140 μl methanesulfonylchloride was added and the mixture was stirred for one hour allowing the temperature to increase to 0° C. Saturated aqueous sodium bicarbonate was added and the mixture was extracted twice with dichloromethane. The organic extracts were combined and dried with sodium sulfate. Evaporation of the solvent gave 308 mg of the title compound as an almost colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829716B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-4a0d51db455349dd85e46800f9f6abac |
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| Source note | uspto-grants-2010_11 |
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