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1-Methylpiperazine → HCID 67457051, 화합물

HRID 1852947
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HRID 1852947 반응식
CS(O[CH2:6][CH2:7][N:8]1[CH:12]=[C:11]([B:13]2[O:17]C(C)(C)C(C)(C)[O:14]2)[CH:10]=[N:9]1)(=O)=O.[CH3:22][N:23]1[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]1>CN(C)C=O.ClCCl>[CH3:22][N:23]1[CH2:28][CH2:27][N:26]([CH2:6][CH2:7][N:8]2[CH:12]=[C:11]([B:13]([OH:14])[OH:17])[CH:10]=[N:9]2)[CH2:25][CH2:24]1
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참가 물질

5

반응물 2

HCID 531671-MethylpiperazineHCID 86685293HCID 86685293, 화합물

생성물 1

HCID 67457051HCID 67457051, 화합물수율 63.2%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 6344Dichloromethane용매

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온도
50 °C

실험 절차

To a solution of 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethyl methanesulfonate (0.080 g, 0.253 mmol) in 0.5 mL N,N-dimethylformamide was added 1-methylpiperazine (0.281 mL, 2.53 mmol) and the reaction was sealed under nitrogen and heated to 50° C. for 2.5 hours. The reaction mixture was diluted with dichloromethane (3 mL) and then loaded directly onto a silica gel column pre-wetted and eluted with 15% methanol in dichloromethane containing 1% ammonium hydroxide to afford 1-(2-(4-methylpiperazin-1-yl)ethyl)-1H-pyrazol-4-ylboronic acid (0.038 g, 0.160 mmol, 63% yield) as a result of hydrolysis on silica in the presence of methanol and ammonium hydroxide. MS (apci) m/z=239.1 (M+H).

후처리

  1. customthe reaction was sealed under nitrogen
  2. washeluted with 15% methanol in dichloromethane containing 1% ammonium hydroxide

출처 및 근거

ORD 기록
ord-5cf00ddb536e42808a82bff6130fbc1c
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962596B2

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