Potassium Carbonate → HCID 86696383、化合物
反応式
Br[C:2]1[N:6]2[N:7]=[C:8]([NH:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH:9]=[CH:10][C:5]2=[N:4][CH:3]=1.B([C:19]1[CH:27]=[CH:26][C:22]([C:23]([OH:25])=[O:24])=[CH:21][CH:20]=1)(O)O.C(=O)([O-])[O-].[K+].[K+]>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(#N)C.O>[CH2:12]([NH:11][C:8]1[CH:9]=[CH:10][C:5]2[N:6]([C:2]([C:19]3[CH:27]=[CH:26][C:22]([C:23]([OH:25])=[O:24])=[CH:21][CH:20]=3)=[CH:3][N:4]=2)[N:7]=1)[CH2:13][CH2:14][CH3:15]参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 145 °C
実験手順
To the mixture of 3-bromo-N-butylimidazo[1,2-b]pyridazin-6-amine (340 mg, 1.26 mmol), 4-boronobenzoic acid (210 mg, 1.26 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (44 mg, 0.063 mmol) and potassium carbonate (261 mg, 1.89 mmol) was added 3:1 acetonitrile/water (3 mL). The resulting mixture was heated at 145° C. (microwave) for 800 s. The reaction was then filtered and concentrated to afford 4-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)benzoic acid (886 mg, >100% yield) as a crude off-white solid: LRMS (ESI) m/e 311.2 [(M+H)+, calcd for C17H19N4O2 311.2].
後処理
- filtrationThe reaction was then filtered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-c88469973ca845369bdb86212189180a
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08969565B2
反応ノート
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