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Potassium Carbonate → HCID 46311864、化合物

HRID 1630746
ノート
印刷プレビュー

反応式

HRID 1630746 の反応式
[F:1][C:2]1[CH:3]=[C:4](B(O)O)[CH:5]=[CH:6][CH:7]=1.COC1C=CC=C(OC)C=1C1C=CC=CC=1P(C1CCCCC1)C1CCCCC1.C(=O)([O-])[O-].[K+].[K+].Cl[C:47]1[C:52]([NH2:53])=[CH:51][CH:50]=[C:49]([CH3:54])[N:48]=1>CC([O-])=O.CC([O-])=O.[Pd+2].O.C(#N)C>[F:1][C:2]1[CH:3]=[C:4]([C:47]2[C:52]([NH2:53])=[CH:51][CH:50]=[C:49]([CH3:54])[N:48]=2)[CH:5]=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 11430Potassium CarbonateHCID 27339863-Fluorophenylboronic acidHCID 27344153-Amino-2-chloro-6-picolineHCID 112698722-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl

生成物 1

HCID 46311864HCID 46311864、化合物

試薬・触媒・溶媒 3

HCID 167845palladium(II) acetate
触媒
HCID 962Water溶媒
HCID 6342Acetonitrile溶媒

反応条件

温度
78 °C

実験手順

To a mixture of 3-fluorophenylboronic acid (1.6 g, 12 mmol), S—PHOS (0.304 g, 0.74 mmol), potassium carbonate (3.41 g, 25 mmol), 2-chloro-6-methylpyridin-3-amine 16 (1.3 g, 9.1 mmol), and Pd(OAc)2 (0.085 g, 0.38 mmol) was added acetonitrile (14 mL) and water (9 mL). The reaction mixture was degassed by bubbling nitrogen through the solution for 10 min and the reaction mixture was heated to 78° C. After 4 h, the reaction mixture was diluted with EtOAc, washed with brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (10% to 50% EtOAc in hexanes) gave 2-(3-fluorophenyl)-6-methylpyridin-3-amine.

後処理

  1. customThe reaction mixture was degassed
  2. customby bubbling nitrogen through the solution for 10 min
  3. additionthe reaction mixture was diluted with EtOAc
  4. washwashed with brine (1×)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification by flash column chromatography on silica gel (10% to 50% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-bf74b374d36e48aba7bccd73ffa7a023
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08791147B2

反応ノート

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