تفاعل #335505

ord-82146073056f4aa1ba339f9fa262aa86

معادلة التفاعل

COc1ccc(C(C)N)cc1
4-methoxy-1-phenylethylamine
CN1CCCCC1
N-methylpiperidine
CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)O
t-butoxycarbonyl-L-valine
CC(C)COC(=O)Cl
isobutyl chloroformate
COc1ccc(C(C)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)cc1
N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide

المذيبات

ظروف التفاعل

درجة الحرارة
-60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىbeing kept below -15° C
  2. 2
    workup.WAITAfter 2 hours at -15° C.
  3. 3
    workup.STIRRINGthe mixture is subsequently stirred at room temperature for 15 hours
  4. 4
    ترشيحthe solid is filtered off
  5. 5
    غسيلrinsed with CH2Cl2
  6. 6
    تركيزthe filtrate is concentrated
  7. 7
    workup.ADDITIONthe residue is introduced into water
  8. 8
    استخلاصthe mixture is extracted twice with ethyl acetate
  9. 9
    غسيلthe combined ethyl acetate phases are washed with NaHCO3 solution and water
  10. 10
    أخرىdried
  11. 11
    تركيزconcentrated

الإجراء التجريبي

2.3 g (0.023 mol) of N-methylpiperidine are added to 5.0 g of t-butoxycarbonyl-L-valine (0.023 mol), dissolved in 50 ml of CH2Cl2, at -20° C. 3.2 g (0.023 mol) of isobutyl chloroformate are then rapidly added dropwise at -20° C., the mixture is subsequently stirred at the same temperature for 10 minutes and cooled to -60° C. and 3.5 g (0.023 mol) of 4-methoxy-1-phenylethylamine are allowed to run in, the temperature being kept below -15° C. After 2 hours at -15° C., the mixture is subsequently stirred at room temperature for 15 hours, the solid is filtered off and rinsed with CH2Cl2, the filtrate is concentrated, the residue is introduced into water, the mixture is extracted twice with ethyl acetate and the combined ethyl acetate phases are washed with NaHCO3 solution and water, dried and concentrated. 17.5 g (85% of theory) of N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide of melting point 126°-127° C. are obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05210084uspto-grants-1993_05