Methanol → 1H-Indole-2,4-dicarboxylic acid 2-tert-butyl ester 4-methyl ester

HRID 1071690노트

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HRID 1071690 반응식
[C:1]([O:5][C:6]([C:8]1[NH:9][C:10]2[C:15]([CH:16]=1)=[C:14](Br)[CH:13]=[CH:12][CH:11]=2)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:18][OH:19].CN([CH:23]=[O:24])C>CCN(CC)CC.CC([O-])=O.CC([O-])=O.[Pd+2].C1(P(C2C=CC=CC=2)[C-]2C=CC=C2)C=CC=CC=1.[C-]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=C1.[Fe+2]>[CH3:18][O:19][C:23]([C:14]1[C:15]2[CH:16]=[C:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[NH:9][C:10]=2[CH:11]=[CH:12][CH:13]=1)=[O:24]

참가 물질

7

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온도
70 °C

실험 절차

To a solution of 7.3 g 4-Bromo-1H-indole-2-carboxylic acid tert-butyl ester in 100 ml DMF, 6.8 ml NEt3, 276 mg Pd(OAc)2, 128 mg 1,1′-Bis(diphenylphosphino)ferrocene, 12 ml MeOH were added and purged with argon for 15 min. This solution was then purged with carbon monoxide and heated to 70° C. for 4 h. The reaction mixture was concentrated under reduced pressure, the residue dissolved in 200 ml DCM and washed with 100 ml water. The organic layer was dried over MgSO4 and, after removal of the solvent under reduced pressure, the residue was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate 9:1. The fractions containing the product were collected and concentrated under reduced pressure.

후처리

  1. custompurged with argon for 15 min
  2. customThis solution was then purged with carbon monoxide
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. dissolutionthe residue dissolved in 200 ml DCM
  5. washwashed with 100 ml water
  6. dry with materialThe organic layer was dried over MgSO4
  7. customafter removal of the solvent under reduced pressure
  8. customthe residue was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate 9:1
  9. additionThe fractions containing the product
  10. customwere collected
  11. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-443db0542ad04468b56af5d85d449233
출처 데이터셋
uspto-grants-2005_06
특허 번호
US06906084B2

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