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Acetic Acid → 3-((4-Methylpiperazin-1-yl)methyl)phenylboronic acid

HRID 1798546
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HRID 1798546 반응식
[CH:1]([C:3]1[CH:4]=[C:5]([B:9]([OH:11])[OH:10])[CH:6]=[CH:7][CH:8]=1)=O.[CH3:12][N:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1.C(O)(=O)C.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>C(Cl)Cl>[CH3:12][N:13]1[CH2:18][CH2:17][N:16]([CH2:1][C:3]2[CH:4]=[C:5]([B:9]([OH:11])[OH:10])[CH:6]=[CH:7][CH:8]=2)[CH2:15][CH2:14]1
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참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 531671-MethylpiperazineHCID 27343563-Formylphenylboronic acidHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 496578973-((4-Methylpiperazin-1-yl)methyl)phenylboronic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 3-Formylphenylboronic acid (1 eq, 2 mmol, 0.3 g) in dry DCM (7 ml) under an inert atmosphere of argon is treated with 1-methyl-piperazine (1.2 eq, 2.4 mmol, 0.266 ml) followed by acetic acid (1.2 eq, 2.4 mmol, 0.14 ml) and NaBH(OAc)3 (1.6 eq, 3.2 mmol, 0.678 mg) and the resulting mixture is stirred at room temperature for 3 hours. The reaction is quenched by addition of water and is then extracted with DCM. The organic extracts are concentrated in vacuo and the crude residue is purified by flash chromatography on silica eluting with MeOH/DCM (0 to 100% MeOH in DCM) followed by 2M NH3 in MeOH. The appropriate fractions are combined and concentrated in vacuo to afford the title compound; [M+H]+=235.

후처리

  1. customThe reaction is quenched by addition of water
  2. extractionis then extracted with DCM
  3. concentrationThe organic extracts are concentrated in vacuo
  4. customthe crude residue is purified by flash chromatography on silica eluting with MeOH/DCM (0 to 100% MeOH in DCM)
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-bc1521ba943942a3a7f84f5aa9f07e31
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08343966B2

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