Dichloromethane → 5-Bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-6-fluoro-1H-indole-7-carboxamide

HRID 656070

반응식

HRID 656070 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:12]([NH2:14])=[O:13])[C:10]=1[F:11])[NH:7][CH:6]=[C:5]2[CH:15]1[CH2:20][CH2:19]S[CH2:17][CH2:16]1.C([O-])(O)=O.[Na+].O[O:27][S:28]([O-:30])=O.[K+].C(Cl)Cl>COCCOC.O.C(N(CC([O-])=O)CC(O)=O)CN(CC([O-])=O)CC(O)=O.[Na+].[Na+]>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:12]([NH2:14])=[O:13])[C:10]=1[F:11])[NH:7][CH:6]=[C:5]2[CH:15]1[CH2:20][CH2:19][S:28](=[O:30])(=[O:27])[CH2:17][CH2:16]1

참가 물질

8

실험 절차

An aqueous solution of 0.0004 M Na2EDTA (0.882 mL, 0.353 μmol) was added to a solution of 5-Bromo-6-fluoro-3-(tetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamide (45 mg, 0.126 mmol) in DME (3 mL). In a separate flask, NaHCO3 (106 mg, 1.260 mmol) was added to a solution of Oxone (232 mg, 0.378 mmol) in water (1 mL). This mixture was then added in 3 portions over 3 min to the DME solution of 5-Bromo-6-fluoro-3-(tetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamide. The reaction was stirred at room temperature for 17 h. Water (2 mL) and DCM (3 mL) were added, the layers were separated, and the aqueous layer was extracted with DCM (3×2 mL). The combined organic layers were washed with saturated NaCl (1×2 mL), dried (Na2SO4), filtered, and concentrated under a stream of nitrogen at 50° C. The residue was dried under high vacuum, giving 9.2 mg (19%) of the title compound.

후처리

  1. customthe layers were separated
  2. extractionthe aqueous layer was extracted with DCM (3×2 mL)
  3. washThe combined organic layers were washed with saturated NaCl (1×2 mL)
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated under a stream of nitrogen at 50° C
  7. customThe residue was dried under high vacuum

출처 및 근거

ORD 기록
ord-12556b0e8983454e9c14b5ad1d08d668
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08071584B2

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