반응 #2256

ord-b2c40033208b4111b3cb9a725ae2825c

반응 방정식

O=C(O)c1cc(-c2ccnc(Nc3cccc(Cl)c3)n2)ccn1
N-[3-chloro-phenyl]-4-(2-carboxy-4-pyridyl)-2-pyrimidineamine
CCN=C=NCCCN(C)C.Cl
N-ethyl-N'-(3-dimethylaminopropyl)-carbodiimide hydrochloride
O=C1CCC(=O)N1O
N-hydroxysuccinimide
NCCN
ethylenediamine
Cl.NCCNC(=O)c1cc(-c2ccnc(Nc3cccc(Cl)c3)n2)ccn1
N-[3-chloro-phenyl]-4-[2-(N-{2-amino-ethyl}-aminocarbonyl)-4-pyridyl]-2-pyrimidineamine hydrochloride

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGAfter stirring for 14 h at RT
  2. 2
    추출extracted with 30 ml of water
  3. 3
    건조The organic phase is dried (sodium sulfate)
  4. 4
    농축concentrated
  5. 5
    기타Crystallisation from isopropanol/ethanolic hydrochloric acid

실험 절차

80 mg (0.24 mmol) of N-[3-chloro-phenyl]-4-(2-carboxy-4-pyridyl)-2-pyrimidineamine, 70.8 mg (0.36 mmol) of N-ethyl-N'-(3-dimethylaminopropyl)-carbodiimide hydrochloride and 42 mg (0.36 mmol) of N-hydroxysuccinimide are dissolved in 3 ml of dimethylformamide and stirred for 2.5 h at RT. The reaction mixture is then added dropwise at 0° within a period of 30 minutes to a solution of 0.77 ml (11.8 mmol) of ethylenediamine in 2 ml of DMF. After stirring for 14 h at RT, the reaction mixture is poured into 50 ml of ethyl acetate and extracted with 30 ml of water. The organic phase is dried (sodium sulfate) and concentrated. Crystallisation from isopropanol/ethanolic hydrochloric acid gives N-[3-chloro-phenyl]-4-[2-(N-{2-amino-ethyl}-aminocarbonyl)-4-pyridyl]-2-pyrimidineamine hydrochloride; m.p. 161°-163°, FAB-MS: 369 (M+ +H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05728708uspto-grants-1998_03