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Tetrahydrofuran → HCID 11649928、化合物

HRID 1911759
ノート
印刷プレビュー

反応式

HRID 1911759 の反応式
C[O-].[Na+].O1CCCC1.[CH:9]1([CH2:13][N:14]([CH2:33][CH3:34])[C:15]2[C:24]([CH2:25][NH:26][C:27]3[CH:31]=[C:30]([CH3:32])[O:29][N:28]=3)=[CH:23][C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]=2)[CH2:12][CH2:11][CH2:10]1.[F:35][C:36]([F:50])([F:49])[C:37]1[CH:38]=[C:39]([CH:42]=[C:43]([C:45]([F:48])([F:47])[F:46])[CH:44]=1)[CH2:40]Br>O.C(OCC)(=O)C>[F:35][C:36]([F:49])([F:50])[C:37]1[CH:38]=[C:39]([CH:42]=[C:43]([C:45]([F:48])([F:46])[F:47])[CH:44]=1)[CH2:40][N:26]([CH2:25][C:24]1[C:15]([N:14]([CH2:13][CH:9]2[CH2:12][CH2:11][CH2:10]2)[CH2:33][CH3:34])=[N:16][C:17]2[C:22]([CH:23]=1)=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:27]1[CH:31]=[C:30]([CH3:32])[O:29][N: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

7

反応物 4

HCID 8028TetrahydrofuranHCID 1225733,5-Bis(trifluoromethyl)benzyl bromideHCID 10942334Sodium MethoxideHCID 57486825HCID 57486825、化合物

生成物 1

HCID 11649928HCID 11649928、化合物収率 20%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8857
Ethyl Acetate
溶媒

実験手順

Sodium methoxide (0.108 g, 2.0 mmol) was added to an anhydrous tetrahydrofuran (6 mL) solution of cyclobutylmethyl-ethyl-{3-[(5-methyl-isoxazol-3-ylamino)-methyl]-quinolin-2-yl}-amine (0.14 g, 0.4 mmol), with stirring, at ambient temperature. After this mixture was stirred for 15 minutes, 3,5-bis-trifluoromethybenzyl bromide (0.08 mL, 0.4 mmol) was added slowly, and stirring was continued overnight. Ethyl acetate (30 mL) and water (30 mL) were added, and the layers were separated. The aqueous layer was back-extracted with ethyl acetate (2×30 mL), and the combined organic extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The crude residue was purified by chromatography on silica gel and eluted with 10-70% hexane in ethyl acetate to afford the title compound (0.045 g, yield: 20%).

後処理

  1. stirringAfter this mixture was stirred for 15 minutes
  2. stirringstirring
  3. customthe layers were separated
  4. extractionThe aqueous layer was back-extracted with ethyl acetate (2×30 mL)
  5. washthe combined organic extracts were washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe crude residue was purified by chromatography on silica gel
  9. washeluted with 10-70% hexane in ethyl acetate

出典と根拠

ORDレコード
ord-3cdd4d8d70f147989bd1c173950b755c
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08604055B2

反応ノート

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