Sodium Iodide → N-(t-butyl)-4-(2-fluoro-5-bromobenzyloxy)butylamine

HRID 1066833ノート

反応式

HRID 1066833 の反応式
[F:1][C:2]1[CH:14]=[CH:13][C:12]([Br:15])=[CH:11][C:3]=1[CH2:4][O:5][CH2:6][CH2:7][CH2:8][CH2:9]Br.[I-].[Na+].[C:18]([NH2:22])([CH3:21])([CH3:20])[CH3:19]>O1CCCC1.C(Cl)Cl>[C:18]([NH:22][CH2:9][CH2:8][CH2:7][CH2:6][O:5][CH2:4][C:3]1[CH:11]=[C:12]([Br:15])[CH:13]=[CH:14][C:2]=1[F:1])([CH3:21])([CH3:20])[CH3:19]

参加物

6

実験手順

A solution of 4-(2-fluoro-5-bromobenzyloxy)butyl bromide (400 mg, 1.18 mmol) in tetrahydrofuran (6 ml) was treated with sodium iodide (242 mg, 1.6 mmol). The resulting mixture was stirred at ambient temperature. After 1.5 hours, the sodium bromide was removed by filtration, and the filtrate concentrated. The residue was treated with a tetrahydrofuran solution of tert-butylamine (1.24 ml, 11.8 mmol). The progress of the reaction was monitored by thin layer chromatography. The resulting mixture was stirred for about 19 hours at ambient temperature. The reaction mixture was diluted with methylene chloride, and washed with saturated sodium bicarbonate. The organic fraction was dried over sodium sulfate and the solvents were removed in vacuo. The desired title intermediate was further purified by radial chromatography.

後処理

  1. customthe sodium bromide was removed by filtration
  2. concentrationthe filtrate concentrated
  3. stirringThe resulting mixture was stirred for about 19 hours at ambient temperature
  4. washwashed with saturated sodium bicarbonate
  5. dry with materialThe organic fraction was dried over sodium sulfate
  6. customthe solvents were removed in vacuo
  7. customThe desired title intermediate was further purified by radial chromatography

出典と根拠

ORDレコード
ord-f279e34001da4ea3964a7a0056214e03
出典データセット
uspto-grants-2001_06
特許番号
US06245761B1

反応ノート

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