반응 #40677

ord-9c1f04891eae4e6f995f2661eafdbac1

반응 방정식

CC(C)(C)CN1CCC2(CC1)CN(c1ccccc1N)c1ccccc12
20f
CC(C)(C)CN1CCC2(CC1)CN(c1ccccc1N)c1ccccc12
2-(1′-neopentylspiro[indoline-3,4′-piperidine]-1-yl)aniline
O=C(N=C=S)c1ccccc1
benzoylisothiocyanate
CC(C)(C)CN1CCC2(CC1)CN(c1ccccc1NC(=S)NC(=O)c1ccccc1)c1ccccc12
N-(2-(1′-neopentylspiro[indoline-3,4′-piperidine]-1-yl)phenylcarbamothioyl)benzamide

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The reaction was concentrated
  2. 2
    기타the residue was purified by flash chromatography (silica gel, 0-10% MeOH/DCM)
  3. 3
    기타to give 20 g

실험 절차

A mixture of 20f (118 mg, 0.33 mmol) and benzoylisothiocyanate (63 μL, 0.47 mmol) in DCM (3 mL) was stirred at rt for 3 h. The reaction was concentrated and the residue was purified by flash chromatography (silica gel, 0-10% MeOH/DCM) to give 20 g, as yellow solid (156 mg). LC-MS m/z 513.06 [M+H]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07728008B2uspto-grants-2010_06