1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde → (Rac)-(1-benzenesulfonyl-1h-pyrrolo[2,3-b]pyridin-3-yl)-[6-(1-methyl-1h-pyrazol-4-yl)imidazo[1,2-b]pyridazin-3-yl]-methanol

HRID 69246ノート

反応式

HRID 69246 の反応式
Br[C:2]1[N:6]2[N:7]=[C:8]([C:11]3[CH:12]=[N:13][N:14]([CH3:16])[CH:15]=3)[CH:9]=[CH:10][C:5]2=[N:4][CH:3]=1.C([Mg]Br)C.[C:21]1([S:27]([N:30]2[C:34]3=[N:35][CH:36]=[CH:37][CH:38]=[C:33]3[C:32]([CH:39]=[O:40])=[CH:31]2)(=[O:29])=[O:28])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C1COCC1>[C:21]1([S:27]([N:30]2[C:34]3=[N:35][CH:36]=[CH:37][CH:38]=[C:33]3[C:32]([CH:39]([C:2]3[N:6]4[N:7]=[C:8]([C:11]5[CH:12]=[N:13][N:14]([CH3:16])[CH:15]=5)[CH:9]=[CH:10][C:5]4=[N:4][CH:3]=3)[OH:40])=[CH:31]2)(=[O:28])=[O:29])[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1

参加物

5

実験手順

3-Bromo-6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazine (Example 8.1, 150 mg, 0.539 mmol) was dissolved in THF (15 mL) under Nitrogen. Ethylmagnesium bromide solution (3 M, 0.360 mL) was added and the mixture was stirred at rt for 30 min. Then 1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (Stage 199.2, 173 mg, 0.539 mmol) in THF (2 mL) was slowly added and the mixture was stirred at rt for 3.5 h. The mixture was quenched with 10% NH4Cl solution. It was extracted with EtOAc twice. The combined organic layers was washed with brine, dried over Na2SO4, filtered and evaporated. The title compound was obtained as a yellow solid (tR 1.4 min (conditions 1), MH+=486).

後処理

  1. stirringthe mixture was stirred at rt for 3.5 h
  2. customThe mixture was quenched with 10% NH4Cl solution
  3. extractionIt was extracted with EtOAc twice
  4. washThe combined organic layers was washed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customevaporated

出典と根拠

ORDレコード
ord-28f63240596541afa69c260f781cc0bf
出典データセット
uspto-grants-2014_09
特許番号
US08822468B2

反応ノート

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