반응 #3985

ord-abd517df60204610939cf68a6c24b096

반응 방정식

NC1CCN(Cc2ccc3ccccc3c2)CC1
4-Amino-1-(naphth-2-ylmethyl)piperidine
O=C(N=C=S)c1ccccc1
benzoylisothiocyanate
O=C(NC(=S)NC1CCN(Cc2ccc3ccccc3c2)CC1)c1ccccc1
1-Benzoyl-3-[1-(naphth-2-ylmethyl)piperid-4-yl]thiourea

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was evaporated
  2. 2
    workup.DISSOLUTIONthe gum dissolved in isopropyl alcohol
  3. 3
    기타The solvent was evaporated
  4. 4
    workup.DISSOLUTIONthe residue dissolved in ethyl acetate
  5. 5
    기타The title compound crystallised
  6. 6
    여과was filtered
  7. 7
    건조dried as the monohydrochloride quarterhydrate salt, m.p. 212°-214° C.

실험 절차

4-Amino-1-(naphth-2-ylmethyl)piperidine (1.0 g, 0.0042 m) and benzoylisothiocyanate (0.69 g, 0.0042 m) in toluene (120 cm3) was stirred at room temperature for 6 hours. The solvent was evaporated and the gum dissolved in isopropyl alcohol and acidified with ethanolic HCl. The solvent was evaporated and the residue dissolved in ethyl acetate. The title compound crystallised and was filtered and dried as the monohydrochloride quarterhydrate salt, m.p. 212°-214° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04722930uspto-grants-1988_02