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

HRID 1798546
ノート
印刷プレビュー

反応式

HRID 1798546 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-bc1521ba943942a3a7f84f5aa9f07e31
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08343966B2

反応ノート

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