Sodium hydride → 4-(2,6-Difluorobenzyl)-6-(1-methyl-2-butynyloxy)pyrimidine

HRID 1592205

反応式

HRID 1592205 の反応式
[H-].[Na+].[CH3:3][CH:4]([OH:8])[C:5]#[C:6][CH3:7].Cl[C:10]1[CH:15]=[C:14]([CH2:16][C:17]2[C:22]([F:23])=[CH:21][CH:20]=[CH:19][C:18]=2[F:24])[N:13]=[CH:12][N:11]=1.[Cl-].[NH4+]>O1CCCC1>[F:24][C:18]1[CH:19]=[CH:20][CH:21]=[C:22]([F:23])[C:17]=1[CH2:16][C:14]1[CH:15]=[C:10]([O:8][CH:4]([CH3:3])[C:5]#[C:6][CH3:7])[N:11]=[CH:12][N:13]=1

参加物

6

反応物 4

HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 1413443-Pentyn-2-olHCID 225997014-Chloro-6-(2,6-difluorobenzyl)pyrimidine

生成物 1

HCID 225998654-(2,6-Difluorobenzyl)-6-(1-methyl-2-butynyloxy)pyrimidine収率 133.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

実験手順

In 1 ml of tetrahydrofuran was suspended 0.04 g of sodium hydride (60% in oil), to which 0.2 ml of a tetrahydrofuran solution containing 0.06 g of 3-pentyn-2-ol was slowly added dropwise under stirring at room temperature. The mixture was stirred at room temperature for 20 minutes, and 0.4 ml of a tetrahydrofuran solution containing 0.15 g of 4-chloro-6-(2,6-difluorobenzyl)pyrimidine was slowly added dropwise at room temperature, followed by stirring for 3 hours. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution and extracted three times with ethyl acetate. The organic layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.24 g of 4-(2,6-difluorobenzyl)-6-(1-methyl-2-butynyloxy)pyrimidine (the present compound (147)).

後処理

  1. additionwas slowly added dropwise
  2. stirringThe mixture was stirred at room temperature for 20 minutes
  3. additionwas slowly added dropwise at room temperature
  4. stirringby stirring for 3 hours
  5. extractionextracted three times with ethyl acetate
  6. washwashed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-0bd4c89b34dc4cd5b25a047b8dd4355c
出典データセット
uspto-grants-2007_11
特許番号
US07291730B2

関連ノート

読み込み中…