Reacción #1361591

Ecuación de reacción

triethylamine

Oxalyl chloride

4-(7-chloroquinolin-4-yl)butan-1-ol

methylsulfoxide

oxalyl chloride

→

title compound

4-(7-Chloroquinolin-4-yl)butyraldehyde

Disolventes

methylene chloride

methylene chloride

methylene chloride

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGthe reaction mixture stirred for another 2.5 hours during which time it
2. 2
   Temperaturawas allowed warmed up to room temperature
3. 3
   OtroThe reaction was quenched by the addition of saturated brine
4. 4
   Otropartitioned with methylene chloride
5. 5
   Extracciónthe methylene chloride extract
6. 6
   Secadodried over anhydrous sodium sulfate powder
7. 7
   Filtraciónfiltered
8. 8
   Concentraciónconcentrated in vacuo

Procedimiento

Oxalyl chloride (0.42 mL of a 2M solution in dry methylene chloride) was placed in an oven-dried flask, cooled to -78° C. and a solution of 99 mg methylsulfoxide in dry methylene chloride (2 mL) added drop by drop to the oxalyl chloride over 3 minutes and stirred for a further 3 minutes. A solution of 4-(7-chloroquinolin-4-yl)butan-1-ol (100 mg) in dry methylene chloride (1 mL) was added to the reaction flask over approx. 3 minutes followed by anhydrous triethylamine (0.42 mL) and the reaction mixture stirred for another 2.5 hours during which time it was allowed warmed up to room temperature. The reaction was quenched by the addition of saturated brine and then partitioned with methylene chloride. The aqueous layer was discarded and the methylene chloride extract dried over anhydrous sodium sulfate powder, filtered and concentrated in vacuo. The title compound was isolated by flash chromatography on silica gel (ethyl acetate:hexane, 2:1; then ethyl acetate), 57 mg.

Fuente