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Sodium borohydride → HCID 21075807、化合物

HRID 1373895
ノート
印刷プレビュー

反応式

HRID 1373895 の反応式
[C:1](=[N:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[CH:9][C:8]=2[N:7]=[C:6]1[CH3:18])([CH3:3])[CH3:2].[BH4-].[Na+]>CO>[CH:1]([NH:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[CH:9][C:8]=2[N:7]=[C:6]1[CH3:18])([CH3:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 21075811HCID 21075811、化合物

生成物 1

HCID 21075807HCID 21075807、化合物収率 100.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution of N-isopropylidene(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)amine (1.82 g, 7.64 mmol) dissolved in 40 mL of MeOH was treated with NaBH4 (1.16 g, 30.6 mmol). After stirring for 18 h, the reaction was quenched with saturated NH4Cl solution and partitioned between CH2Cl2 and 2% Na2CO3 solution. The organic portion was washed with 2% Na2CO3 solution, H2O and brine and dried over Na2SO4. The resulting organic portion was filtered and concentrated under reduced pressure to give N-isopropyl(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)amine (1.84 g) as a yellow foam.

後処理

  1. customthe reaction was quenched with saturated NH4Cl solution
  2. custompartitioned between CH2Cl2 and 2% Na2CO3 solution
  3. washThe organic portion was washed with 2% Na2CO3 solution, H2O and brine
  4. dry with materialdried over Na2SO4
  5. filtrationThe resulting organic portion was filtered
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-8c65c9cc8f5c4e89a42f0ed34fb7c749
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07163947B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート