반응 #2468010

ord-de4459fe418c4107ab0138afcc27f787

반응 방정식

CN(C)c1cnc(Cl)nc1N1CCc2nc[nH]c2C1
2-chloro-4-(3,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-5-dimethylamino-pyrimidine
O
water
Cl
hydrochloric acid
CN(C)Cc1ccc(N)cc1
4-dimethylaminomethyl-phenylamine
CN(C)Cc1ccc(Nc2ncc(N(C)C)c(N3CCc4nc[nH]c4C3)n2)cc1
2-(4-dimethylaminomethyl-phenylamino)-4-(3,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-5-dimethylamino-pyrimidine

반응 조건

온도
95°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The suspension obtained
  2. 2
    기타purified by column chromatography
  3. 3
    기타The fractions are freeze-dried
  4. 4
    기타freeze-dried once more

실험 절차

50 mg 2-chloro-4-(3,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-5-dimethylamino-pyrimidine are suspended in 60 μL of 1,4-dioxane, 20 μL water and 90 μL of a 5 M hydrochloric acid (in 1,4-dioxane) and mixed with 55 mg 4-dimethylaminomethyl-phenylamine. This mixture is heated to 95° C. and stirred for 20 h at this temperature. The suspension obtained is diluted with DMF and then purified by column chromatography. The carrier material used is C18-RP-silica gel and a gradient is run through which consists at the starting point of 95% water (10 mM ammonium hydrogen carbonate and 38 mM ammonia) and 5% acetonitrile and at the finishing point of 50% water and 50% acetonitrile. The fractions are freeze-dried. The residue is taken up in acetonitrile, combined with aqueous hydrochloric acid and freeze-dried once more.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08258129B2uspto-grants-2012_09