Ethanol → HCID 59639635, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]3[CH:21]=[CH:20][C:19](=[O:22])[N:18]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=4[F:29])[C:10]=3[N:11]=[C:12](S(C)(=O)=O)[N:13]=2)=[C:4]([CH3:30])[CH:3]=1.[H-].[Na+].[CH3:33][CH2:34][OH:35]>>[CH2:34]([O:35][C:12]1[N:13]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][C:4]=2[CH3:30])[C:9]2[CH:21]=[CH:20][C:19](=[O:22])[N:18]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=3[F:29])[C:10]=2[N:11]=1)[CH3:33]Participants
4
Procedure
The product of Example 59 (200 mg, 0.47 mmol) was placed in EtOH (10 mL) and the mixture stirred under Ar. Approximately 2 mL of the ethanol was distilled off to dry the mixture. When the mixture was cooled to 23°, some of the starting material sulfone crystallized out. NaH (11.5 mg, 0.46 mmol) was added. The reaction did not go to completion, so additional NaH (4 mg, 0.16 mmol) was added. The solvent was removed in vacuo, and the residue was flash chromatographed on silica gel eluted with 60-100% CH2Cl2/hexane. Recrystallization from CH2Cl2/hexane gave the title compound as a white crystalline solid. mp 137-139°, LC MS m/z=394(MH+) Retention time=2.32 min.
Workup
- distillationApproximately 2 mL of the ethanol was distilled off
- customto dry the mixture
- temperatureWhen the mixture was cooled to 23°
- customsome of the starting material sulfone crystallized out
- additionwas added
- customThe solvent was removed in vacuo
- customchromatographed on silica gel
- washeluted with 60-100% CH2Cl2/hexane
- customRecrystallization from CH2Cl2/hexane
Sources & evidence
- ORD record
- ord-dfb55af449b7416b8a808a234762c9cc
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07314934B2
Reaction notes
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