Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 15-Crown-5 | HCID 36336 | — |
| Reactant | 2-Chloropyridine-3-sulfonyl chloride | HCID 10219968 | — |
| Reactant | tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate | HCID 67176761 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86624001 | HCID 86624001 | 91% |
Reaction Steps
To a suspension of sodium hydride (60% in oil, 39 mg) in tetrahydrofuran (6 mL) were added dropwise 15-crown-5 (0.19 mL), a solution of tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (243 mg) in tetrahydrofuran (1 mL) and 2-chloropyridine-3-sulfonyl chloride (239 mg) under ice-cooling, and the mixture was stirred for 0.5 hr. The reaction mixture was diluted with water, and extracted with ethyl acetate. The separated aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→3:7) to give the title compound as a pale-yellow oil (yield 340 mg, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08933105B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-6a5bf37dcd334ad596d5ffe517d19986 |
|---|
| Source note | uspto-grants-2015_01 |
|---|