Реакция #84063

ord-3219bbed21a1411293876a5c8f2bfaf0

Уравнение реакции

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
Выход 46.0%

Растворители

Условия реакции

Температура
110°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwas degassed three times under N2 atmosphere
  2. 2
    Фильтрацияfiltered
  3. 3
    ПромывкаThe filtrate was washed with brine (20 mL)
  4. 4
    Сушкаdried over Na2SO4
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09433618B2uspto-grants-2016_09