反応 #84058

ord-4827d6c016174071b5a561081304ea89

反応方程式

Cl
HCl
COCCOCCO
DEGME
COc1ccc2nc(Cl)c(C)cc2c1
2-chloro-6-methoxy-3-methylquinoline
OB(O)c1ccc(-c2nnn[nH]2)cc1
4-(1H-tetrazol-5-yl)phenylboronic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
COc1ccc2nc(-c3ccc(-c4nnn[nH]4)cc3)c(C)cc2c1
desired product
収率 84.0%
COc1ccc2nc(-c3ccc(-c4nnn[nH]4)cc3)c(C)cc2c1
2-(4-(1H-tetrazol-5-yl)phenyl)-6-methoxy-3-methylquinoline
収率 84.0%

溶媒

反応条件

温度
150°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The solids were filtered

実験手順

To a mixture of 2-chloro-6-methoxy-3-methylquinoline (100 mg, 0.482 mmol), 4-(1H-tetrazol-5-yl)phenylboronic acid (91.2 mg, 0.482 mmol), K2CO3 (199 mg, 1.45 mmol), and PdCl2(dppf) (17.6 mg, 0.024 mmol) was added 7 mL of DEGME and 3 mL of H2O under argon. The mixture was stirred at 150° C. in a microwave reactor for 1.5 hours. The crude mixture was diluted with 1N NaOH (10 mL) and slowly acidified to a pH of 4.0 using conc. HCl. The solids were filtered to yield 128 mg (84% yield) of desired product.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09433618B2uspto-grants-2016_09