반응 #1252

ord-564b28fa70ee43db9e87ffa6d6c4d4e6

반응 방정식

COc1ccccc1
anisole
O=C(O)C(F)(F)F
trifluoroacetic acid
CC1(NC(=O)OC(C)(C)C)CCN(c2nccc(Cl)n2)CC1
4-t-butoxycarbonylamino-1-(4-chloropyrimidin-2-yl)-4-methylpiperidine
[Na+].[OH-]
NaOH
CC1(N)CCN(c2nccc(Cl)n2)CC1
4-amino-1-(4-chloropyrimidin-2-yl)-4-methylpiperidine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출The reaction medium is extracted with methylene chloride
  2. 2
    건조dried over Na2SO4
  3. 3
    기타the solvent and the anisole are evaporated off under reduced pressure
  4. 4
    기타The residue is purified by chromatography

실험 절차

A solution of 2.22 g (0.0068 mol) of 4-t-butoxycarbonylamino-1-(4-chloropyrimidin-2-yl)-4-methylpiperidine (step c) in 25 ml of anhydrous methylene chloride is cooled under a nitrogen atmosphere and 5 ml of anisole and 25 ml of trifluoroacetic acid are added slowly. The mixture is stirred for 1 hour at room temperature and 25 ml of a 30% solution of NaOH are added slowly. The reaction medium is extracted with methylene chloride and dried over Na2SO4 and the solvent and the anisole are evaporated off under reduced pressure. The residue is purified by chromatography using CH2Cl2 /MeOH=9/1 as the eluent to give 4-amino-1-(4-chloropyrimidin-2-yl)-4-methylpiperidine as the base, which is treated with maleic acid in an ethanol/isopropyl ether mixture. The maleate obtained in this way is isolated by filtration (m.p. 154°-155° C.).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723611uspto-grants-1998_03