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Water → 2,4-Bis(methyloxy)-5-(2-methyl-1,3-thiazol-4-yl)pyrimidine

HRID 1925022
ノート
印刷プレビュー

反応式

HRID 1925022 の反応式
Br[C:2]1[N:3]=[C:4]([CH3:7])[S:5][CH:6]=1.[CH3:8][O:9][C:10]1[N:15]=[C:14]([O:16][CH3:17])[C:13](B(O)O)=[CH:12][N:11]=1.O.C([O-])(O)=O.[Na+]>COCCOC.ClCCl>[CH3:8][O:9][C:10]1[N:15]=[C:14]([O:16][CH3:17])[C:13]([C:2]2[N:3]=[C:4]([CH3:7])[S:5][CH:6]=2)=[CH:12][N:11]=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 4

HCID 962WaterHCID 516892Sodium BicarbonateHCID 2736209(2,4-Dimethoxypyrimidin-5-yl)boronic acidHCID 27631864-Bromo-2-methyl-1,3-thiazole

生成物 1

HCID 594483562,4-Bis(methyloxy)-5-(2-methyl-1,3-thiazol-4-yl)pyrimidine

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒
HCID 8071
1,2-Dimethoxyethane
溶媒

反応条件

温度
90 °C

実験手順

4-bromo-2-methyl-1,3-thiazole (commercially available from Frontier, 300 mg, 1.685 mmol) was dissolved in 1,2-Dimethoxyethane (DME) (5 ml). Pd(Ph3)4 (97 mg, 0.084 mmol) was added and the reaction mixture was stirred at room temperature for 15 min. [2,4-bis(methyloxy)-5-pyrimidinyl]boronic acid (commercially available from Aldrich, 651 mg, 3.54 mmol) and 1M/H2O sol. of NaHCO3 (4.60 ml, 4.60 mmol) were added thereto. The reaction mixture was heated at 90° C. for 2.5 h and left at room temperature overnight. The mixture was then diluted with dichloromethane (20 ml) and washed with water (20 ml). The organic layer was separated through an hydrophobic frit and concentrated. The obtained crude was purified by flash chromatography eluting with Cyclohexane/AcOEt 8/2. 290 mg of the title compound were isolated as a white solid.

後処理

  1. additionwere added
  2. washwashed with water (20 ml)
  3. customThe organic layer was separated through an hydrophobic frit
  4. concentrationconcentrated
  5. customThe obtained crude
  6. customwas purified by flash chromatography
  7. washeluting with Cyclohexane/AcOEt 8/2

出典と根拠

ORDレコード
ord-ccc0413084de4899a032057559aca432
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08178549B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート