Réaction #716069

Équation de réaction

2-chloro-6-methoxyquinoline

5-cyanothiophen-2-ylboronic acid

sodium carbonate

→

5-(6-hydroxyquinolin-2-yl)thiophene-2-carbonitrile

Solvants

DME

Conditions de réaction

Traitement

1. 1
   Autrethe two step synthesis
2. 2
   AutreIn step 2, after quenching w/ ice water
3. 3
   Extractiona standard ethyl acetate extraction
4. 4
   Autrewas preformed followed by purification by prep-TLC (PE:EA=1:1)

Mode opératoire

Followed the two step synthesis shown in Scheme 1 starting with 2-chloro-6-methoxyquinoline and 5-cyanothiophen-2-ylboronic acid, with minor variations: the base used in step 1 was sodium carbonate and the solvent was DME (dimethoxyethane)/water. In step 2, after quenching w/ ice water, a standard ethyl acetate extraction was preformed followed by purification by prep-TLC (PE:EA=1:1).

Source