تفاعل #84062

ord-550c1e91025842e7bcb55db1293d04a9

معادلة التفاعل

CCOC(=O)C1CCNCC1
Ethyl piperidine-4-carboxylate
COc1ccc2nc(Cl)ccc2c1
2-chloro-6-methoxyquinoline
COc1ccc2nc(Cl)ccc2c1
Intermediate 1
COc1ccc2nc(Cl)ccc2c1
2-chloro-6-methoxyquinoline
CC#N
MeCN
CCOC(=O)C1CCC(c2ccc3cc(OC)ccc3n2)CC1
ethyl 4-(6-methoxyquinolin-2-yl)cyclohexanecarboxylate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter aqueous work-up with EtOAc and column purification
  2. 2
    غسيلeluting with EtOAc/hexane

الإجراء التجريبي

Ethyl piperidine-4-carboxylate (100 mg) was treated with 2-chloro-6-methoxyquinoline (Intermediate 1) (90 mg) in MeCN (0.8 mL) and TEA (100 mg) in a sealed tube at 180° C. for 6 h in a microwave reactor. After aqueous work-up with EtOAc and column purification, eluting with EtOAc/hexane, ethyl 4-(6-methoxyquinolin-2-yl)cyclohexanecarboxylate (90 mg) was afforded as a solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09433618B2uspto-grants-2016_09