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2-Aminopyridine → 5-[3-(2-Chloro-4-pyrimidinyl)imidazo[1,2-a]pyridin-2-yl]-2-(methyloxy)-benzonitrile

HRID 419306
ノート
印刷プレビュー

反応式

HRID 419306 の反応式
[Cl:1][C:2]1[N:7]=[C:6]([CH2:8][C:9]([C:11]2[CH:12]=[CH:13][C:14]([O:19][CH3:20])=[C:15]([CH:18]=2)[C:16]#[N:17])=O)[CH:5]=[CH:4][N:3]=1.Cl[C:22]1[N:27]=[C:26](/[CH:28]=[C:29](/[C:31]2C=CC(OC)=C(C=2)C#N)\O)C=C[N:23]=1.C1C(=O)N(Br)C(=O)C1.NC1C=CC=CN=1.C([O-])(O)=O.[Na+]>C(Cl)Cl>[Cl:1][C:2]1[N:7]=[C:6]([C:8]2[N:27]3[CH:26]=[CH:28][CH:29]=[CH:31][C:22]3=[N:23][C:9]=2[C:11]2[CH:12]=[CH:13][C:14]([O:19][CH3:20])=[C:15]([CH:18]=2)[C:16]#[N:17])[CH:5]=[CH:4][N:3]=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

7

反応物 5

HCID 104392-AminopyridineHCID 67184N-bromobutanimideHCID 516892Sodium BicarbonateHCID 594527625-[(2-Chloro-4-pyrimidinyl)acetyl]-2-(methyloxy)benzonitrileHCID 1360784795-[(Z)-2-(2-chloro-4-pyrimidinyl)-1-hydroxyethenyl]-2-(methyloxy)benzonitrile

生成物 1

HCID 59452778
5-[3-(2-Chloro-4-pyrimidinyl)imidazo[1,2-a]pyridin-2-yl]-2-(methyloxy)-benzonitrile
収率 65%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
65 °C

実験手順

To a tautomeric mixture of 5-[(2-chloro-4-pyrimidinyl)acetyl]-2-(methyloxy)benzonitrile and 5-[(Z)-2-(2-chloro-4-pyrimidinyl)-1-hydroxyethenyl]-2-(methyloxy)benzonitrile (2.87 g, 10.0 mmol) in DCM (250 mL) was added NBS (1.78 g, 10.0 mmol) in one portion. Upon completion by TLC, the reaction was concentrated. The residue was taken up in dioxane (100 mL) and 2-aminopyridine (2.89 g, 30.7 mmol) was added. The reaction was stirred at 65° C. overnight. The reaction was poured into half saturated NaHCO3, extracted with DCM and EtOAc, dried (MgSO4), concentrated and triturated with diethyl ether to provide the title compound (2.36 g, 6.50 mmol, 65%). 1H NMR (400 MHz, DMSO-d6) δ ppm 3.96 (s, 3H), 7.18-7.25 (m, 2H), 7.33 (d, J=9.0 Hz, 1H), 7.52-7.58 (m, 1H), 7.77 (d, J=9.0 Hz, 1H), 7.92 (dd, J=8.8, 2.4 Hz, 1H), 8.00 (d, J=2.2 Hz, 1H), 8.56 (d, J=5.5 Hz, 1H), 9.34-9.39 (m, 1H).

後処理

  1. concentrationUpon completion by TLC, the reaction was concentrated
  2. extractionextracted with DCM and EtOAc
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated
  5. customtriturated with diethyl ether

出典と根拠

ORDレコード
ord-e6278c44c88347c3a67109938e2b9762
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093239B2

反応ノート

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