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Methanol → Methyl 3-(4-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)phenyl)-2-(4-(diethoxymethyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate

HRID 1467543
ノート
印刷プレビュー

反応式

HRID 1467543 の反応式
[CH:1]1([C:4]([N:6]2[CH2:11][CH2:10][N:9]([C:12]([C:14]3[CH:21]=[CH:20][C:17](C=O)=[CH:16][CH:15]=3)=[O:13])[CH2:8][CH2:7]2)=[O:5])[CH2:3][CH2:2]1.[CH2:22]([O:24][CH:25]([O:44][CH2:45][CH3:46])[C:26]1[CH:43]=[CH:42][C:29]([CH:30]=[N:31][C:32]2[CH:40]=[CH:39][CH:38]=[C:37]3[C:33]=2[CH2:34][O:35][C:36]3=[O:41])=[CH:28][CH:27]=1)[CH3:23].[CH3:47][O-:48].[Na+].[CH3:50]O>C(OCC)(=O)CC>[CH:1]1([C:4]([N:6]2[CH2:11][CH2:10][N:9]([C:12]([C:14]3[CH:21]=[CH:20][C:17]([CH:50]4[C:47](=[O:48])[C:33]5[C:37]([C:36]([O:35][CH3:34])=[O:41])=[CH:38][CH:39]=[CH:40][C:32]=5[NH:31][CH:30]4[C:29]4[CH:28]=[CH:27][C:26]([CH:25]([O:44][CH2:45][CH3:46])[O:24][CH2:22][CH3:23])=[CH:43][CH:42]=4)=[CH:16][CH:15]=3)=[O:13])[CH2:8][CH2:7]2)=[O:5])[CH2:2][CH2:3]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 887MethanolHCID 10942334Sodium MethoxideHCID 672585054-(4-(diethoxymethyl)benzylideneamino)isobenzofuran-1(3H)-oneHCID 866390294-(4-(Cyclopropanecarbonyl)piperazine-1-carbonyl)benzaldehyde

生成物 1

HCID 67258880Methyl 3-(4-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)phenyl)-2-(4-(diethoxymethyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate
収率 26%

試薬・触媒・溶媒 1

HCID 7749Ethyl Propionate溶媒

反応条件

温度
0 °C

実験手順

A mixture of 4-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)benzaldehyde (859 mg, 3 mmol) and 4-(4-(diethoxymethyl)benzylideneamino)isobenzofuran-1(3H)-one (1.018 g, 3 mmol) in ethyl propionate (40 mL) was cooled to 0° C. Then a solution of sodium methoxide in methanol [sodium (276 mg, 12 mmol) in methanol (8 mL)] was added dropwise. After the addition, the mixture was stirred at room temperature for 20 hr. The mixture was quenched with water (10 mL) and solvent was removed in vacuum. The residue was dissolved in water, and then extracted with ethyl acetate (100 mL×4). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and concentrated to give crude product. The crude product was purified by chromatography (silica gel, petroleum ether/ethyl acetate=10:1 to 1:10) to give methyl 3-(4-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)phenyl)-2-(4-(diethoxymethyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate (500 mg, yield 26%). LC-MS (ESI) m/z: 640 (M+1)+.

後処理

  1. additionAfter the addition
  2. customThe mixture was quenched with water (10 mL) and solvent
  3. customwas removed in vacuum
  4. dissolutionThe residue was dissolved in water
  5. extractionextracted with ethyl acetate (100 mL×4)
  6. washThe combined organic layers were washed with brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated
  9. customto give crude product
  10. customThe crude product was purified by chromatography (silica gel, petroleum ether/ethyl acetate=10:1 to 1:10)

出典と根拠

ORDレコード
ord-e536b9c4dca848b491599edcd32630a2
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08999987B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート