تفاعل #685024

ord-f009d28e78c04276a7da1ea5be3ef8c9

معادلة التفاعل

N#CC1CCN(C(=O)OCc2ccccc2)CC1
benzyl 4-cyanopiperidine-1-carboxylate
CC(C)(C)[Si](C)(C)I.CCCC
iodo-tert-butyldimethylsilane butane
C1CCOC1
THF
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
LiHMDS
CC(C)(C)[Si](C)(C)OCCCCC1(C#N)CCN(C(=O)OCc2ccccc2)CC1
title compound
المردود 67.0%
CC(C)(C)[Si](C)(C)OCCCCC1(C#N)CCN(C(=O)OCc2ccccc2)CC1
Benzyl 4-(4-(tert-butyldimethylsilyloxy)butyl)-4-cyanopiperidine-1-carboxylate
المردود 67.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter quenching with water
  2. 2
    workup.ADDITIONthe organic phase was diluted with EtOAc
  3. 3
    غسيلwashed with water, brine
  4. 4
    تجفيفdried (Na2SO4)
  5. 5
    تركيزAfter concentration
  6. 6
    أخرىthe residue was purified by flash chromatography (10% to 20% EtOAc/hexane)

الإجراء التجريبي

To a stirred solution of benzyl 4-cyanopiperidine-1-carboxylate (10 g, 41 mmol) and iodo-tert-butyldimethylsilane butane (12.6 mL, 49 mmol) in THF (80 mL) cooled to −78° C. was added LiHMDS (50 mL, 50 mmol, 1M in THF) dropwise over 30 min. The resulting mixture was stirred while gradually warming to room temperature for 18 h. After quenching with water, the organic phase was diluted with EtOAc and washed with water, brine and dried (Na2SO4). After concentration, the residue was purified by flash chromatography (10% to 20% EtOAc/hexane) to give the title compound as yellow oil (11.88 g, 67% yield). 1H NMR (300 MHz, CDCl3) δ: 7.34-7.28 (5H, m), 5.09 (2H, s), 4.17 (2H, bs), 3.59 (2H, t, J=5.3 Hz), 3.07 (2H, bs), 1.89 (2H, d, J=13.2 Hz), 1.53 (6H, bs), 1.43-1.34 (2H, m), 0.85 (9H, s), 0.01 (6H, s). LCMS (M+H): 431.20.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897593B2uspto-grants-2011_03