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Borane → 3-Methyl-N2-(4-quinolyl)butane-1,2-diamine

HRID 333052
ノート
印刷プレビュー

反応式

HRID 333052 の反応式
[CH3:1][CH:2]([CH3:18])[CH:3]([NH:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=[CH:10][CH:9]=1)[C:4]([NH2:6])=O.B>C1COCC1>[CH3:1][CH:2]([CH3:18])[CH:3]([NH:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=[CH:10][CH:9]=1)[CH2:4][NH2:6]
参加物反応条件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 6331BoraneHCID 668354133-Methyl-2-(4-quinolylamino)butanamide

生成物 1

HCID 651919333-Methyl-N2-(4-quinolyl)butane-1,2-diamine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

3-Methyl-2-(4-quinolylamino)butanamide (460 mg, 1.9 mmol) was dissolved in anhydrous THF (30 ml) under argon, the mixture was cooled to 0° C. and a 1M solution of borane in anhydrous THF (8 ml, 8 mmol) was added with stirring. Stirring was continued for 1 hour at 0° C., the cooling bath was removed and the mixture was allowed to warm to room temperature overnight with stirring. The mixture was quenched with 1M NaOH and extracted with ethyl acetate. The organic phase was evaporated to dryness under reduced pressure and the residue was purified by column chromatography (pre-packed silica column, gradient of ethyl acetate/methanol containing 1% ammonia). 220 mg was obtained (0.96 mmol, 51%). MS (APCI) m/z=229.8 [M+H]+.

後処理

  1. stirringStirring
  2. customthe cooling bath was removed
  3. temperatureto warm to room temperature overnight
  4. stirringwith stirring
  5. customThe mixture was quenched with 1M NaOH
  6. extractionextracted with ethyl acetate
  7. customThe organic phase was evaporated to dryness under reduced pressure
  8. customthe residue was purified by column chromatography (pre-packed silica column, gradient of ethyl acetate/methanol containing 1% ammonia)
  9. custom220 mg was obtained (0.96 mmol, 51%)

出典と根拠

ORDレコード
ord-0d1befbb89b84c088279b5edcb6197f7
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08877934B2

反応ノート

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