Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 178490698 | HCID 178490698 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178490699 | HCID 178490699 | 88% |
Reaction Steps
A mixture of the product of Example 163 (220 mg, 0.6 mmol) in CH2Cl2 (20 mL) and triethylamine (181 mg, 1.8 mmol) was cooled to 0° C., and treated dropwise with methanesulfonyl chloride (102 mg, 0.9 mmol). The reaction was stirred at 0° C. for 30 min., poured into water, and the mixture was extracted with CH2Cl2 (2×). The organics were combined, dried over MgSO4, filtered and concentrated to afford the title compound (234 mg, 88%). MS (DCI/NH3) m/z 383 (M−Ms+15)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501794B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-f5ba6602257b49a29f1730ce346ee3b4 |
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| Source note | uspto-grants-2013_08 |
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