Water → 4-(Benzyloxy)pyridin-3-amine

HRID 595690ノート

反応式

HRID 595690 の反応式
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][N:12]=[CH:11][C:10]=1[N+:15]([O-])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH4+].[Cl-].C1COCC1.O>CO.[Fe]>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][N:12]=[CH:11][C:10]=1[NH2:15])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

7

反応物 4

HCID 962WaterHCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 127165204-(Benzyloxy)-3-nitropyridine

生成物 1

HCID 288900524-(Benzyloxy)pyridin-3-amine収率 81.8%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 887Methanol溶媒

実験手順

To a solution of 4-(benzyloxy)-3-nitropyridine (42.0 g, 0.18 mol), Fe (30.6 g, 0.55 mol) and NH4Cl (48.8 g, 0.91 mol) in MeOH:THF:H2O=(2:2:1, 750 mL) was stirred at reflux for 3 h. After being filtered and concentrated in vacuum, the residue was purified by column chromatography (DCM:MeOH=10:1) to give to give the pure 4-(benzyloxy)pyridin-3-amine (29.5 g, yield: 80.7%). 1H-NMR (CDCl3, 400 MHz) δ 8.25 (s, 1H), 7.88 (s, 1H), 7.20˜7.65 (m, 5H), 6.89 (s, 1H), 5.18 (s, 2H). MS (M+H)+: 201.

後処理

  1. temperatureat reflux for 3 h
  2. filtrationAfter being filtered
  3. concentrationconcentrated in vacuum
  4. customthe residue was purified by column chromatography (DCM:MeOH=10:1)
  5. customto give

出典と根拠

ORDレコード
ord-94c13b9f600b44dca61f47db0cee8982
出典データセット
uspto-grants-2016_01
特許番号
US09243002B2

反応ノート

読み込み中…