반응 #1253

ord-b6be6f155af94436ba0e8bfe5bd8a6cd

반응 방정식

COc1ccccc1
anisole
O=C(O)C(F)(F)F
trifluoroacetic acid
CC1(NC(=O)OC(C)(C)C)CCN(c2ccnc(Cl)n2)CC1
4-t-butoxycarbonylamino-1-(2-chloropyrimidin-4-yl)-4-methylpiperidine
[Na+].[OH-]
NaOH
CC1(N)CCN(c2ccnc(Cl)n2)CC1
4-amino-1-(2-chloropyrimidin-4-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

실험 절차

The procedure described in Example 2 is followed up to the end of step (c). A solution of 6.81 g (0.021 mol) of 4-t-butoxycarbonylamino-1-(2-chloropyrimidin-4-yl)-4-methylpiperidine (step c) in 80 ml of anhydrous methylene chloride is cooled under a nitrogen atmosphere and 16.4 ml of anisole and 83 ml of trifluoroacetic acid are added slowly. The mixture is stirred for 1 hour at room temperature and 80 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 to give 4-amino-1-(2-chloropyrimidin-4-yl)-4-methylpiperidine as the base, which is treated with maleic acid in an ethanol/ethyl ether mixture. The maleate obtained in this way is isolated by filtration (yield 65%, m.p. 125°-126° C.).

출처

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