Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 90281431 | HCID 90281431 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90281516 | HCID 90281516 | — |
Reaction Steps
Compound 41C (35.6 mg, 0.06 mmol) was dissolved in 1 mL of methylene chloride and cooled to 0° C. To it was added 0.2 mL of pyridine followed by methanesulfonyl chloride (0.007 mL, 0.09 mmol). The reaction mixture was stirred at 0° C. for one hour. LCMS showed complete reaction. It was then partitioned between EtOAc and brine. The organic layer was separated, dried and concentrated to afford the title product. MS (m/z) 670.27 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09050344B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-4ff334f34e7e441fa0855bbdfe348843 |
|---|
| Source note | uspto-grants-2015_06 |
|---|