تفاعل #2446122

ord-e459a2e7196146c0b480b13ad27c7f8a

معادلة التفاعل

N[C@@H](Cc1ccc(O)c2ncccc12)C(=O)O
3-(8-hydroxyquinolin-5-yl)alanine
O=S(Cl)Cl
thionyl chloride
CCO
ethanol
CCOC(=O)[C@@H](N)Cc1ccc(O)c2ncccc12
3-(8-hydroxyquinolin-5-yl)alanine ethyl ester
المردود 92.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةrefluxed overnight
  2. 2
    أخرىThe solution was evaporated to dryness in vacuum
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in absolute ethanol
  4. 4
    أخرىreevaporated to dryness
  5. 5
    أخرىwas further purified by FC(CH2Cl2:MeOH:AcOH 9:1.5:1.5)

الإجراء التجريبي

To a stirred slurry of DL-3-(8-hydroxyquinolin-5-yl)alanine (HLM8) (2.19 g, 7.04 mmol) in absolute ethanol (26 ml) at 0° C., with protection from atmospheric moisture by CaCl2 tube in N2, thionyl chloride was added dropwise (1.1 ml, 14.1 mmol). The reaction mixture was stirred at 0° C. for 30 minutes and at room temperature for 30 minutes, and then refluxed overnight. The solution was evaporated to dryness in vacuum. The residue was dissolved in absolute ethanol and reevaporated to dryness. To ensure completeness of the esterification, the whole operation was repeated. The ester HLM9 (yellow solid, 1.67 g, 92% yield), which was shown by HPLC to contain about 1% of free amino acid, was further purified by FC(CH2Cl2:MeOH:AcOH 9:1.5:1.5). 1H NMR (250 MHz, D2O) 0.94 (dd, J=7.2, 7.2 Hz, 3H), 3.63 (m, 2H), 4.01 (m, 2H), 4.34 (dd, J=7.7, 7.5 Hz, 1H), 7.31 (d, J=8.0 Hz, 1H), 7.56 (d, J=8.2 Hz, 1H), 8.01 (dd, J=8.7, 5.4 Hz, 1H), 8.93 (d, J=5.4 Hz, 1H), 9.08 (d, J=8.7 Hz, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685955B2uspto-grants-2014_04