Tetrahydrofuran → 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid 4-((E)-2-carboxy-vinyl)-phenyl ester

HRID 1008125ノート

反応式

HRID 1008125 の反応式
[CH3:1][C:2]1[CH:6]=[C:5]([CH3:7])[NH:4][C:3]=1/[CH:8]=[C:9]1\[C:10](=[O:25])[N:11]([C:18](N2C=CN=C2)=[O:19])[C:12]2[C:17]\1=[CH:16][CH:15]=[CH:14][CH:13]=2.[C:26]([OH:36])(=[O:35])[CH:27]=[CH:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.C1C[O:40]CC1>C(N(CC)CC)C>[C:26](/[CH:27]=[CH:28]/[C:29]1[CH:30]=[CH:31][C:32]([O:40][C:18]([N:11]2[C:12]3[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=3)/[C:9](=[CH:8]/[C:3]3[NH:4][C:5]([CH3:7])=[CH:6][C:2]=3[CH3:1])/[C:10]2=[O:25])=[O:19])=[CH:33][CH:34]=1)([OH:36])=[O:35]

参加物

5

反応物 3

HCID 8028TetrahydrofuranHCID 87842-Propenoic acid, 3-phenyl-HCID 601112313-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-1-(imidazol-1-ylcarbonyl)-1,3-dihydro-indol-2-one

生成物 1

HCID 601112193-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid 4-((E)-2-carboxy-vinyl)-phenyl ester収率 16%

試薬・触媒・溶媒 1

HCID 8471Triethylamine触媒

反応条件

温度
60 °C

実験手順

A reaction mixture of of 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1-(imidazol-1-ylcarbonyl)-1,3-dihydro-indol-2-one (165 mg, 0.5 mmol), cinnamic acid (85 mg, 0.5 mmol), and 2 drops of triethylamine in 3 mL of THF was stirred at 60° C. for 5 h and room temperature overnight and filtered. The solid was then washed with ethyl acetate and 1 N aqueous hydrogen chloride solution. The filtrate was concentrated and the residue was partitioned between ethyl acetate and water-acetic acid. The organic layer was washed with diluted sodium hydroxide solution, dried over magnesium sulfate, and concentrated. The resultant residue was suspended in warm ethyl acetate and filtered. The combined solid was then dried in a vacuum oven overnight to afford 35 mg (16%) of 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid 4-((E)-2-carboxy-vinyl)-phenyl ester. 1H NMR (400 MHz, DMSO-d6) δ 12.55 (s, 1H, NH-1′), 12.41 (s, br, 1H, COOH), 7.91-7.94 (m, 1H), 7.82-7.85 (m, 3H), 7.71 (s, 1H, H-vinyl), 7.65 (d, J=6.02 Hz, 1H), 7.44 (d, J=8.99 Hz, 1H), 7.24-7.26 (m, 2H), 6.57 (d, J=6.02 Hz, 1H), 6.15 (d, J=2.35 Hz, 1H, H-4′), 2.39 (s, 3H, CH3), and 2.37 (s, 3H, CH3).

後処理

  1. filtrationfiltered
  2. washThe solid was then washed with ethyl acetate and 1 N aqueous hydrogen chloride solution
  3. concentrationThe filtrate was concentrated
  4. customthe residue was partitioned between ethyl acetate and water-acetic acid
  5. washThe organic layer was washed with diluted sodium hydroxide solution
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated
  8. filtrationfiltered
  9. customThe combined solid was then dried in a vacuum oven overnight

出典と根拠

ORDレコード
ord-30e844a182a54f9ab2272ed3b682c156
出典データセット
uspto-grants-2004_09
特許番号
US06797725B2

反応ノート

読み込み中…