Sodium Bicarbonate → N-Phenyl-N'-{4-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1-(tetrahydro-2-furanylmethyl)-1H-pyrazol-3-yl]phenyl}urea

HRID 1727701노트

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HRID 1727701 반응식
Br[C:2]1[C:3]([C:13]2[CH:18]=[CH:17][C:16]([NH:19][C:20]([NH:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[O:21])=[CH:15][CH:14]=2)=[N:4][N:5]([CH2:7][CH:8]2[CH2:12][CH2:11][CH2:10][O:9]2)[CH:6]=1.C1(S([N:38]2[C:42]3=[N:43][CH:44]=[CH:45][C:46](B4OC(C)(C)C(C)(C)O4)=[C:41]3[CH:40]=[CH:39]2)(=O)=O)C=CC=CC=1.C(=O)(O)[O-].[Na+]>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CN(C)C=O>[C:23]1([NH:22][C:20]([NH:19][C:16]2[CH:17]=[CH:18][C:13]([C:3]3[C:2]([C:46]4[CH:45]=[CH:44][N:43]=[C:42]5[NH:38][CH:39]=[CH:40][C:41]=45)=[CH:6][N:5]([CH2:7][CH:8]4[CH2:12][CH2:11][CH2:10][O:9]4)[N:4]=3)=[CH:14][CH:15]=2)=[O:21])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

참가 물질

6

반응물 3

HCID 516892Sodium BicarbonateHCID 450745461-(Benzenesulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridineHCID 68996099HCID 68996099, 화합물

생성물 1

HCID 57398440N-Phenyl-N'-{4-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1-(tetrahydro-2-furanylmethyl)-1H-pyrazol-3-yl]phenyl}urea수율 11%

시약·촉매·용매 2

HCID 178418397HCID 178418397, 화합물촉매HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

A mixture of N-{4-[4-bromo-1-(tetrahydro-2-furanylmethyl)-1H-pyrazol-3-yl]phenyl}-N′-phenylurea (0.147 mmol), 1-(phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine (0.162 mmol), N,N-dimethylformamide (1.5 mL), saturated aqueous sodium bicarbonate (0.44 mL) and tetrakis(triphenylphosphine)palladium(0) (0.007 mmol) in a sealed tube was stirred at 100° C. for 18 hrs. The solution was cooled to room temperature, filtered though Celite and concentrated in vacuo. The residue was dissolved in methanol (5 mL) and 6.0N aqueous sodium hydroxide (1 mL) and stirred at 70° C. for 6 h. The reaction mixture was concentrated in vacuo, dissolved in water (10 mL) and extracted with ethyl acetate (3×10 mL). The combined organic extracts were dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by Gilson reverse phase HPLC afforded the title compound as a white solid (11%). ESMS [M+H]+: 479.4

후처리

  1. temperatureThe solution was cooled to room temperature
  2. filtrationfiltered though Celite
  3. concentrationconcentrated in vacuo
  4. dissolutionThe residue was dissolved in methanol (5 mL)
  5. stirring6.0N aqueous sodium hydroxide (1 mL) and stirred at 70° C. for 6 h
  6. concentrationThe reaction mixture was concentrated in vacuo
  7. dissolutiondissolved in water (10 mL)
  8. extractionextracted with ethyl acetate (3×10 mL)
  9. dry with materialThe combined organic extracts were dried over magnesium sulfate
  10. concentrationconcentrated in vacuo
  11. customPurification of the residue by Gilson reverse phase HPLC

출처 및 근거

ORD 기록
ord-6135f548a566462385f0712151293037
출처 데이터셋
uspto-grants-2009_02
특허 번호
US07495102B2

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