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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
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HRID 2090290 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 6386tert-Butanol용매2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-8f3ef6f38a214724ae47b6a9697fcfc6
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436008B2

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