Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 68453819 | HCID 68453819 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86749741 | HCID 86749741 | 98.6% |
Reaction Steps
A solution of 2.88 g(7.28 mmol) of the alcohol 2 in 32 mL dichloromethane at 0° C. was treated with 1.29 g(1.77 mL, 12.7 mmol) of triethylamine followed by addition of 1.04 g(0.70 mL, 9.10 mmol) of methanesulfonylchloride. The solution was stirred at 0° C. for 15 min, followed by dilution with dichloromethane and extraction with water. The solution was dried (Na2SO4) and concentrated in vacuo to afford 3.4 g(98%) of the mesylate 3 as a light pink solid (high resolution mass spectrum: calcd for C20H28FN3O7S: 473.1632. found: 473.1631), sufficiently pure for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05700799 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-7e7353f8a50348bfa8541952f0b9ce65 |
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| Source note | uspto-grants-1997_12 |
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