반응 #84099

ord-0b27d0a7cdd5423ba2dae8f19cc7abac

반응 방정식

COc1ccc2nc(Cl)ccc2c1
2-chloro-6-methoxyquinoline
COC(=O)c1ccc(B(O)O)c(N)c1
2-amino-4-(methoxycarbonyl)phenylboronic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)c(N)c1
product
수율 19.0%
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)c(N)c1
methyl 3-amino-4-(6-methoxyquinolin-2-yl)benzoate
수율 19.0%

반응 조건

온도
80°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출After aqueous workup with EtOAc extraction
  2. 2
    기타the resulting crude product was purified by silica gel column (PE/EtOAc=15/1 to 3/1)

실험 절차

To a mixture of compound 2-chloro-6-methoxyquinoline (1.70 g, 8.78 mmol), 2-amino-4-(methoxycarbonyl)phenylboronic acid (2.05 g, 10.5 mmol), and K2CO3 (2.43 g, 17.6 mmol) in ethylene glycol monomethyl ether/H2O (35 mL/5 mL) was added Pd(dppf)Cl2 (158 mg, 0.193 mmol) under N2 atmosphere. Then the mixture was heated to 80° C. for 3 hours. After aqueous workup with EtOAc extraction, the resulting crude product was purified by silica gel column (PE/EtOAc=15/1 to 3/1) to give the product (500 mg, yield 19%) as a yellow solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09433618B2uspto-grants-2016_09