反应 #84063

ord-3219bbed21a1411293876a5c8f2bfaf0

反应方程式

COc1ccc2nc(Cl)ccc2c1
2-chloro-6-methoxyquinoline
COc1ccc2nc(Cl)ccc2c1
Intermediate 1
COc1ccc2nc(Cl)ccc2c1
2-chloro-6-methoxyquinoline
O=C(O)c1ccc(B(O)O)c(Cl)c1
4-carboxy-2-chlorophenylboronic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
收率 46.0%

反应条件

温度
110°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他was degassed three times under N2 atmosphere
  2. 2
    过滤filtered
  3. 3
    洗涤The filtrate was washed with brine (20 mL)
  4. 4
    干燥dried over Na2SO4
  5. 5
    过滤filtered
  6. 6
    浓缩concentrated

实验过程

A mixture of 2-chloro-6-methoxyquinoline (Intermediate 1) (200 mg, 1.04 mmol), 4-carboxy-2-chlorophenylboronic acid (247 mg, 1.24 mmol) and K2CO3 (369 mg, 2.70 mmol) in DEGME/H2O (7.0 mL/2.0 mL) was degassed three times under N2 atmosphere. Then PdCl2(dppf) (75 mg, 0.104 mmol) was added and the mixture was heated to 110° C. for 3 hours under N2 atmosphere. The reaction mixture was diluted with EtOAc (100 mL) and filtered. The filtrate was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give 3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid (150 mg, yield 46%) as a yellow solid, which was used for the next step without further purification.

来源

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