تفاعل #220772

ord-664513ffdb3d42019888ccb8997ce83a

معادلة التفاعل

O=C(O)CNC(=O)OCC1c2ccccc2-c2ccccc21
N-(9-fluorenylmethyloxycarbonyl)glycine
CCN=C=NCCCN(C)C
EDCI
On1nnc2ccccc21
HOBt
CC(C)(C)OC(=O)N1CCC(CN)CC1
4-(aminomethyl)-1-(tert-butoxycarbonyl)piperidine
CC(C)(C)OC(=O)N1CCC(CNC(=O)CNC(=O)OCC2c3ccccc3-c3ccccc32)CC1
1-(tert-butoxycarbonyl)-4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine
المردود 44.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe resulting reaction mixture
  2. 2
    غسيلwashed with water (100 mL×3) and brine (100 mL×2)
  3. 3
    تجفيفdried over anhydrous sodium sulfate
  4. 4
    تركيزconcentrated
  5. 5
    أخرىrecrystallized from acetonitrile/methanol (150 mL/1 mL) at 0° C.

الإجراء التجريبي

Triethylamine (3.51 g), N-(9-fluorenylmethyloxycarbonyl)glycine (7.93 g, 26.7 mmol), EDCI (3.80 g) and HOBt (4.33 g) were added to a dichloromethane (150 mL) solution of 4-(aminomethyl)-1-(tert-butoxycarbonyl)piperidine (5.72 g). The resulting reaction mixture was stirred at room temperature for 18 hours, then washed with water (100 mL×3) and brine (100 mL×2), dried over anhydrous sodium sulfate, concentrated and recrystallized from acetonitrile/methanol (150 mL/1 mL) at 0° C. to provide 1-(tert-butoxycarbonyl)-4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine (5.75 g, 44%) as an off-white crystal.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07390830B1uspto-grants-2008_06