Sodium Carbonate → 4-(8-(Cyclobutylamino)-[1,2,4]triazolo[1,5-a]pyrazin-5-yl)furan-2-carboxamide

HRID 1093961

반응식

HRID 1093961 반응식
Br[C:2]1[N:7]2[N:8]=[CH:9][N:10]=[C:6]2[C:5]([NH:11][CH:12]2[CH2:15][CH2:14][CH2:13]2)=[N:4][CH:3]=1.CC1(C)C(C)(C)OB([C:24]2[CH:25]=[C:26]([C:29]([NH2:31])=[O:30])[O:27][CH:28]=2)O1.C(=O)([O-])[O-].[Na+].[Na+]>C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd].[Pd].[Pd].[Pd].O1CCOCC1>[CH:12]1([NH:11][C:5]2[C:6]3[N:7]([N:8]=[CH:9][N:10]=3)[C:2]([C:24]3[CH:25]=[C:26]([C:29]([NH2:31])=[O:30])[O:27][CH:28]=3)=[CH:3][N:4]=2)[CH2:15][CH2:14][CH2:13]1

참가 물질

6

반응 조건

온도
90 °C

실험 절차

The product of Step 1 (900 mg, 3.35 mmol), Intermediate 5 (4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-furan-2-carboxylic acid amide, 1.8 g, 4.02 mmol), tetrakis palladium triphenylphosphine (970 mg, 0.84 mmol), sodium carbonate solution (1.5 M, 18 mL, 26.8 mmol) and dioxane (20 mL) are combined in a flask. The mixture is degassed with nitrogen for 10 min then sealed and heated at 90° C. for 18 h. The reaction mixture is cooled and the precipitate collected by filtration. The precipitate is washed with 2% methanol: dichloromethane (2 mL) to give the title compound as a white solid (910 mg, 91%). 1H-NMR (400 MHz, d6-DMSO) =1.74-1.76 (m, 2H), 2.22-2.26 (m, 2H), 2.32 (brs, 2H), 4.70 (brd, 1H, J=7.6), 7.58 (s, 1H), 7.86 (s, 1H), 7.97 (s, 1H), 8.12 (s, 1H), 8.35 (d, 1H, J=7.2), 8.69 (d, 11H, J=9.6). LCMS: Rt 2.63 min (90.4%), m/z (APCI) 299 (M+H)+.

후처리

  1. customThe mixture is degassed with nitrogen for 10 min
  2. customthen sealed
  3. temperatureThe reaction mixture is cooled
  4. filtrationthe precipitate collected by filtration
  5. washThe precipitate is washed with 2% methanol

출처 및 근거

ORD 기록
ord-5fe68fceb45e4aa9983e0f7c82f52b11
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08133895B2

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