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Dichloromethane → HCID 21941423、化合物

HRID 1158885
ノート
印刷プレビュー

反応式

HRID 1158885 の反応式
CC(C[AlH]CC(C)C)C.C(Cl)Cl.C([O:15][C:16]([C:18]1[N:19]=[C:20]2[CH2:25][N:24]([CH2:26][C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[CH2:23][CH2:22][N:21]2[CH:33]=1)=O)C>C1(C)C=CC=CC=1>[CH2:26]([N:24]1[CH2:23][CH2:22][N:21]2[CH:33]=[C:18]([CH:16]=[O:15])[N:19]=[C:20]2[CH2:25]1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6344DichloromethaneHCID 14487Diisobutylaluminum hydrideHCID 68442225HCID 68442225、化合物

生成物 1

HCID 21941423HCID 21941423、化合物

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

1.01 M solution of DIBAL in toluene (1 mL+0.2 mL+0.3 mL) was added to the dry CH2Cl2 (5 mL) solution of 7-benzyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylic acid ethyl ester (283 mg) under a nitrogen atmosphere at −78° C. and stirred for 1.5 h. The mixture was quenched with 1 M HCl (5 mL). The reaction mixture was filtered through a pad of Celite. The filtrate was washed with 50% K2CO3 aq. and the aqueous layer was extracted with CH2Cl2. The combined organic layer was dried (K2CO3) and filtered. The filtrate was concentrated under reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with CHCl3-acetone (9/1˜4/1) and CHCl3-MeOH (19/1). The titled compound was obtained as colorless crystals (148 mg, 61%).

後処理

  1. customThe mixture was quenched with 1 M HCl (5 mL)
  2. filtrationThe reaction mixture was filtered through a pad of Celite
  3. washThe filtrate was washed with 50% K2CO3 aq.
  4. extractionthe aqueous layer was extracted with CH2Cl2
  5. dry with materialThe combined organic layer was dried (K2CO3)
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated under reduced pressure
  8. washthe column was eluted with CHCl3-acetone (9/1˜4/1) and CHCl3-MeOH (19/1)

出典と根拠

ORDレコード
ord-b8c3f0a30131469785e1e7e3ef7d8f3b
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07812014B2

反応ノート

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