Sodium Carbonate → HCID 23624542, 화합물

HRID 389044

반응식

HRID 389044 반응식
Cl[C:2]1[N:3]=[N:4][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH:14]3[CH2:16][CH2:15]3)[CH2:10][CH2:9]2)=[CH:6][CH:7]=1.C(=O)([O-])[O-].[Na+].[Na+].[CH2:23]1[O:31][C:30]2[CH:29]=[CH:28][C:27](B(O)O)=[CH:26][C:25]=2[O:24]1>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(#N)C>[O:24]1[C:25]2[CH:26]=[CH:27][C:28]([C:2]3[N:3]=[N:4][C:5]([N:8]4[CH2:13][CH2:12][N:11]([CH:14]5[CH2:16][CH2:15]5)[CH2:10][CH2:9]4)=[CH:6][CH:7]=3)=[CH:29][C:30]=2[O:31][CH2:23]1

참가 물질

6

반응 조건

온도
80 °C

실험 절차

3-Chloro-6-(4-cyclopropylpiperazin-1-yl)pyridazine (8.0 g, 33.5 mmol), acetonitrile (100 mL), 1 M sodium carbonate solution (100.5 mL, 100.5 mmol) and bis(triphenylphosphine)palladium(II) chloride (1.17 g, 1.67 mmol) were mixed and degassed in vacuo under nitrogen. 3,4-Methylenedioxybenzeneboronic acid (8.34 g, 50.3 mmol) was added and the mixture was heated to 80° C. for 16 h. The precipitated product was filtered and washed with acetonitrile and water, and dried in vacuo. The solid was suspended in methanol (500 mL) and 2,2 equivalents of a 4M HCl in dioxane solution was added. The formed solution was filtered, concentrated in vacuo and acetonitrile (100 mL) was added. The suspension was stirred for 1 h, filtered and the solid dried in vacuo to yield 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)pyridazine as a yellow powder, 11.4 g, 86%.

후처리

  1. customdegassed in vacuo under nitrogen
  2. filtrationThe precipitated product was filtered
  3. washwashed with acetonitrile and water
  4. customdried in vacuo
  5. addition2,2 equivalents of a 4M HCl in dioxane solution was added
  6. filtrationThe formed solution was filtered
  7. concentrationconcentrated in vacuo and acetonitrile (100 mL)
  8. additionwas added
  9. filtrationfiltered
  10. customthe solid dried in vacuo

출처 및 근거

ORD 기록
ord-98a5652ec5814fc58020b88c343717e9
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08378097B2

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