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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole → 2-Ethoxy-5-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine

HRID 2090290
ノート
印刷プレビュー

反応式

HRID 2090290 の反応式
[CH3:1][C:2]1([CH3:14])[C:6]([CH3:8])([CH3:7])[O:5][B:4]([C:9]2[CH:10]=[N:11][NH:12][CH:13]=2)[O:3]1.CC(C)([O-])C.[K+].Cl[CH2:22][C:23]1[CH:24]=[CH:25][C:26]([O:29][CH2:30][CH3:31])=[N:27][CH:28]=1>C(O)(C)(C)C>[CH2:30]([O:29][C:26]1[CH:25]=[CH:24][C:23]([CH2:22][N:12]2[CH:13]=[C:9]([B:4]3[O:5][C:6]([CH3:7])([CH3:8])[C:2]([CH3:14])([CH3:1])[O:3]3)[CH:10]=[N:11]2)=[CH:28][N:27]=1)[CH3:31]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 27740104-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 105351905-(CHLOROMETHYL)-2-ETHOXYPYRIDINEHCID 23665647Potassium tert-butoxide

生成物 1

HCID 594023392-Ethoxy-5-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine

試薬・触媒・溶媒 1

HCID 6386tert-Butanol溶媒2 回

実験手順

To a mixture of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.58 g, 3.0 mmol, Aldrich, Cat. 525057) in tert-butyl alcohol (5.0 mL) was added a solution of potassium tert-butoxide in tert-butyl alcohol (5.0 mL, 5.0 mmol, 1.00 M, Aldrich Cat. 331341). The reaction mixture was stirred at r.t. for 10 minutes followed by an addition of 5-(chloromethyl)-2-ethoxypyridine (0.54062 g, 3.15 mmol). The reaction mixture was stirred at 65° C. overnight. The reaction mixture was cooled to r.t., quenched with aqueous ammonium chloride, and extracted with EtOAc. The combined organic layers were washed with water and brine successively, dried with MgSO4, and concentrated. The residue was purified by flash chromatograph on a silica gel column using 20% ethyl acetate in methylene chloride as eluent to afford the desired compound. LCMS (M+H)+: m/z=330.4.

後処理

  1. stirringThe reaction mixture was stirred at 65° C. overnight
  2. temperatureThe reaction mixture was cooled to r.t.
  3. customquenched with aqueous ammonium chloride
  4. extractionextracted with EtOAc
  5. washThe combined organic layers were washed with water and brine successively
  6. dry with materialdried with MgSO4
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatograph on a silica gel column

出典と根拠

ORDレコード
ord-8f3ef6f38a214724ae47b6a9697fcfc6
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08436008B2

反応ノート

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