Reaktion #1691858

Reaktionsgleichung

2-(4-tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochloride

benzyl indole-3-carboxylate

triethylamine

N,N-dimethylpropylenediamine

→

benzyl 1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]carbonyl}indole-3-carboxylate

Ausbeute 77.6%

Lösungsmittel

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturunder reflux for 7 hours
2. 2
   WaschenThe dichloromethane solution was washed with brine
3. 3
   Trocknendried over magnesium sulfate
4. 4
   Einengenconcentrated under reduced pressure
5. 5
   Wascheneluted with a mixture of n-hexane and ethyl acetate
6. 6
   workup.ADDITIONThe fractions containing the objective compound
7. 7
   Einengenconcentrated under reduced pressure

Vorschrift

A mixture of 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochloride (140 mg), benzyl indole-3-carboxylate (73.3 mg), triethylamine (0.089 ml) and N,N-dimethylaminopyridine (4 mg) in dichloromethane (4 ml) was stirred under reflux for 7 hours. After being cooled to room temperature, the mixture was treated with N,N-dimethylpropylenediamine (0.018 ml) and diluted with dichloromethane. The dichloromethane solution was washed with brine, dried over magnesium sulfate and concentrated under reduced pressure. The resulting residue was subjected to column chromatography on silica gel and eluted with a mixture of n-hexane and ethyl acetate. The fractions containing the objective compound were combined and concentrated under reduced pressure to give benzyl 1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]carbonyl}indole-3-carboxylate (121 mg).

Quelle