Acetone → 6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-(2-methanesulfonyl-ethyl)-3H-benzoimidazole-5-carbaldehyde

[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-(2-methanesulfonyl-ethyl)-3H-benzoimidazol-5-yl]-methanol 10y (0.050, 0.105 mmol) is dissolved in 1:1 THF:acetone (2 mL) under N2 and MnO2 (0.046 g, 0.524 mmol) is added. The reaction mixture is stirred at room temperature for 16 hours, and then at 55° C. for 5 hours. Additional MnO2 (0.046 g, 0.524 mmol) is added and the reaction mixture stirred at 55° C. for 2 hours. The reaction mixture is concentrated to dryness and the residue dissolved in 10:1 methylene chloride:MeOH. The solution is filtered through a silica gel plug eluted with 10:1 methylene chloride:MeOH. The resulting filtrate is concentrated under reduced pressure to give 41 mg (82%) desired product as a bright yellow solid.

1. waitat 55° C. for 5 hours
2. stirringthe reaction mixture stirred at 55° C. for 2 hours
3. concentrationThe reaction mixture is concentrated to dryness
4. dissolutionthe residue dissolved in 10:1 methylene chloride
5. filtrationThe solution is filtered through a silica gel plug
6. washeluted with 10:1 methylene chloride
7. concentrationThe resulting filtrate is concentrated under reduced pressure

ORDレコード

ord-89289b11fe3e4548b83b894bbf117487

出典データセット

uspto-grants-2012_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08193229B2