반응 #1697982

ord-1aa582c3a4cc4ab0a7f765ae600bc7f6

반응 방정식

CC(C)(C)OC(=O)NCC1CCNCC1
4-(N-tert-butyloxycarbonylaminomethyl) piperidine
CSC(=N)NC(=O)OCc1ccccc1
N-benzyloxycarbonyl-S-methylisothiourea
CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
title product
수율 37.0%
CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
4-(N-tert-butyloxycarbonylaminomethyl)-1-(N-benzyloxycarbon ylamidino)piperidine
수율 37.0%

용매

반응 조건

온도
65°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was evaporated
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in CH2Cl2
  3. 3
    세척The organic layer was washed twice with 0.3 M KHSO4 and once with brine
  4. 4
    건조The combined organic layer was dried (Na2SO4)
  5. 5
    여과filtered
  6. 6
    기타evaporated
  7. 7
    기타The crude product was purified by flash chromatography

실험 절차

7.8 g (36.4 mmole) of 4-(N-tert-butyloxycarbonylaminomethyl) piperidine and 8.98 g (40 mmole) of N-benzyloxycarbonyl-S-methylisothiourea was mixed in 25 mL ethanol. The mixture was heated at 60-70° C. for six hours and left at roomtemperature for two days. The solvent was evaporated and the residue was dissolved in CH2Cl2. The organic layer was washed twice with 0.3 M KHSO4 and once with brine. The combined organic layer was dried (Na2SO4), filtered and evaporated. The crude product was purified by flash chromatography using a stepwise gradient of CH2Cl2/MeOH (100/0, 97/3, 95/5, 90/10) as eluent to yield 5.22 g (37%) of the title product.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06984627B1uspto-grants-2006_01