Sulfuryl chloride → HCID 59292845、化合物
反応式
S(Cl)([Cl:4])(=O)=O.[CH2:6]([O:8][C:9]([C:11]1[CH:12]=[CH:13][C:14]([C:21]2[CH:26]=[C:25]([O:27][CH3:28])[CH:24]=[C:23]([O:29][CH3:30])[C:22]=2[F:31])=[C:15]2[C:20]=1[N:19]=[CH:18][CH:17]=[CH:16]2)=[O:10])[CH3:7]>CC#N>[CH2:6]([O:8][C:9]([C:11]1[CH:12]=[CH:13][C:14]([C:21]2[C:22]([F:31])=[C:23]([O:29][CH3:30])[CH:24]=[C:25]([O:27][CH3:28])[C:26]=2[Cl:4])=[C:15]2[C:20]=1[N:19]=[CH:18][CH:17]=[CH:16]2)=[O:10])[CH3:7]参加物
反応条件
- 温度
- -20 °C
実験手順
Sulfuryl chloride (75 μL, 0.93 mmol) was added dropwise to a cold (−20° C.) solution of 5-(2-fluoro-3,5-dimethoxy-phenyl)-quinoline-8-carboxylic acid ethyl ester (Step 176.3) (330 mg, 0.93 mmol) in CH3CN (6 mL). The reaction mixture was stirred for 10 min at −20° C., quenched by addition of a saturated solution of NaHCO3, and concentrated. The residue was diluted in EtOAc and a saturated solution of NaHCO3. The aqueous phase was separated and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography (Hex/EtOAc, 3:2) to provide 240 mg of the title compound as a white solid. Title compound: ESI-MS: 390.1 [M+H]+; tR=3.98 min (System 1); TLC: Rf=0.15 (Hex/EtOAc, 3:2).
後処理
- customquenched by addition of a saturated solution of NaHCO3
- concentrationconcentrated
- additionThe residue was diluted in EtOAc
- customThe aqueous phase was separated
- extractionextracted with EtOAc
- washThe combined organic layers were washed with H2O and brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by silica gel column chromatography (Hex/EtOAc, 3:2)
出典と根拠
- ORDレコード
- ord-c4f20a8bc2d64e1292e19bcd271ccedc
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08674099B2
反応ノート
読み込み中…