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2-Bromoaniline → ethyl 7-bromo-3-(3-ethoxy-3-oxopropyl)-1H-indole-2-carboxylate

HRID 2199710
ノート
印刷プレビュー

反応式

HRID 2199710 の反応式
[Br:1][C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].N([O-])=[O:10].[Na+].[C:13]([O-])(=O)[CH3:14].[Na+].[CH2:18]([O:20][C:21]([CH:23]1[CH2:27][CH2:26][CH2:25][C:24]1=[O:28])=[O:22])[CH3:19]>Cl.O>[Br:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]2[C:3]=1[NH:4][C:25]([C:24]([O:28][CH2:13][CH3:14])=[O:10])=[C:26]2[CH2:27][CH2:23][C:21]([O:20][CH2:18][CH3:19])=[O:22]
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

7

反応物 4

HCID 119922-BromoanilineHCID 69136Ethyl 2-oxocyclopentanecarboxylateHCID 517045Sodium AcetateHCID 23668193Sodium Nitrite

生成物 1

HCID 68940416ethyl 7-bromo-3-(3-ethoxy-3-oxopropyl)-1H-indole-2-carboxylate

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒
HCID 962
Water
溶媒
3 回

反応条件

温度
19 °C

実験手順

A mixture of 2-bromoaniline (34.2 g) in 5M HCl (50 mL) and water (250 mL) at 0° C. was treated with NaNO2 (13.8 g) in water (200 mL). After addition, sodium acetate (92.3 g) in water (250 mL) and 2-oxo-cyclopentanecarboxylic acid ethyl ester (30 mL) were added. The mixture was stirred for 15 minutes, warmed to 19° C. over two hours and extracted with dichloromethane. The extract was dried (MgSO4), filtered and concentrated. The concentrate was dissolved in 1.1:1 H2SO4:ethanol (30 mL), refluxed overnight, cooled to room temperature, quenched with water (1.5 L), and filtered. The filtrant was dissolved in dichloromethane (200 mL) and filtered through a Flash 75 cartridge with dichloromethane. After concentration, the product was recrystallized from hexane.

後処理

  1. additionwere added
  2. extractionextracted with dichloromethane
  3. dry with materialThe extract was dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. dissolutionThe concentrate was dissolved in 1.1:1 H2SO4
  7. temperatureethanol (30 mL), refluxed overnight
  8. temperaturecooled to room temperature
  9. customquenched with water (1.5 L)
  10. filtrationfiltered
  11. dissolutionThe filtrant was dissolved in dichloromethane (200 mL)
  12. filtrationfiltered through a Flash 75 cartridge with dichloromethane
  13. concentrationAfter concentration
  14. customthe product was recrystallized from hexane

出典と根拠

ORDレコード
ord-6502f330eecf471d84a49b8233d2caad
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09359296B2

反応ノート

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