تفاعل #1605827

ord-a202d3dff2e74614a50a00e69ee14a52

معادلة التفاعل

C[N+]1(C)CCC(OC(=O)Nc2cc(CCCCCCCCCNC[C@H](O)c3ccc(OCc4ccccc4)c4[nH]c(=O)ccc34)ccc2-c2ccccc2)CC1.O=C([O-])C(F)(F)F
4-({[5-(9-[{(2R)-[8-(benzyloxy)-2-oxo-1,2-dihydroquinolin-5-yl]-2-hydroxyethyl}amino]nonyl)-2-phenylphenyl]carbamoyl}oxy)-1,1-dimethylpiperidin-1-ium trifluoroacetate
C[N+]1(C)CCC(OC(=O)Nc2cc(CCCCCCCCCNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)ccc2-c2ccccc2)CC1.O=C([O-])C(F)(F)F
4-({[5-(9-{[(2R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl]amino}nonyl)-2-phenylphenyl]carbamoyl}oxy)-1,1-dimethylpiperidin-1-ium trifluoroacetate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe reaction solution was filtered through celite
  2. 2
    تركيزthe filtrate was concentrated under reduced pressure
  3. 3
    أخرىThe residue was purified by HPLC fractionation

الإجراء التجريبي

The obtained 4-({[5-(9-[{(2R)-[8-(benzyloxy)-2-oxo-1,2-dihydroquinolin-5-yl]-2-hydroxyethyl}amino]nonyl)-2-phenylphenyl]carbamoyl}oxy)-1,1-dimethylpiperidin-1-ium trifluoroacetate was dissolved in methanol (5 mL), 10% palladium-carbon (50 mg) was added thereto, and the mixture was stirred under a hydrogen atmosphere at room temperature for 2 hours. The reaction solution was filtered through celite and the filtrate was concentrated under reduced pressure. The residue was purified by HPLC fractionation to obtain 4-({[5-(9-{[(2R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl]amino}nonyl)-2-phenylphenyl]carbamoyl}oxy)-1,1-dimethylpiperidin-1-ium trifluoroacetate (12.79 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09072734B2uspto-grants-2015_07