Butylimidazole → 9-Cyano-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid ethyl ester

HRID 84635

Reaktionsgleichung

Reaktionsgleichung von HRID 84635
[CH2:1]([O:3][C:4]([C:6]1[S:7][C:8]2[CH2:9][CH2:10][O:11][C:12]3[CH:19]=[CH:18][C:17](Br)=[CH:16][C:13]=3[C:14]=2[N:15]=1)=[O:5])[CH3:2].[CH2:21]([N:25]1C=CN=C1)CCC>C1(C)C=CC=CC=1.[Fe-4](C#N)(C#N)(C#N)(C#N)(C#N)C#N.[K+].[K+].[K+].[K+].[Cu]I>[CH2:1]([O:3][C:4]([C:6]1[S:7][C:8]2[CH2:9][CH2:10][O:11][C:12]3[CH:19]=[CH:18][C:17]([C:21]#[N:25])=[CH:16][C:13]=3[C:14]=2[N:15]=1)=[O:5])[CH3:2]

Komponenten

6

Versuchsvorschrift

A mixture of 9-bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid ethyl ester (500 mg), potassium ferrocyanide (dried, 104 mg), copper (I) iodide (27 mg) and 1-butylimidazole (0.37 mL) in toluene (3 mL) was reacted in the microwave at 160° C. for 4 h. The mixture was then partitioned between dichloromethane (30 mL) and water (20 mL). The organic layer was dried (MgSO4), reduced in vacuo and purified on silica to give 9-cyano-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid ethyl ester.

Aufarbeitung

  1. customwas reacted in the microwave at 160° C. for 4 h
  2. customThe mixture was then partitioned between dichloromethane (30 mL) and water (20 mL)
  3. dry with materialThe organic layer was dried (MgSO4)
  4. custompurified on silica

Quellen und Nachweise

ORD-Eintrag
ord-f93db726695745e9b2a4f1d416c38efe
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846762B2

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