반응 #163700

ord-62e6c91e556f4d4c9ceec62fa63016f4

반응 방정식

Oc1cccc(Nc2ncc(F)c(Nc3cccc(O)c3)n2)c1
N2,N4-bis(3-hydroxyphenyl)-5-fluoro-2,4-pyrimidinediamine
FC(F)(F)c1cnc(Cl)nc1Cl
2,4-dichloro-5-trifluoromethylpyrimidine
CCOC(=O)Cc1ccc(N)cc1
ethyl 4-aminophenylacetate
CCOC(=O)Cc1ccc(Nc2ncc(C(F)(F)F)c(Nc3ccc(CC(=O)OCC)cc3)n2)cc1
N2,N4-bis[4-(ethoxycarbonylmethyl)phenyl]-5-trifluoromethyl-2,4-pyrimidinediamine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타were reacted

실험 절차

In a manner similar to the preparation of N2,N4-bis(3-hydroxyphenyl)-5-fluoro-2,4-pyrimidinediamine, 2,4-dichloro-5-trifluoromethylpyrimidine and ethyl 4-aminophenylacetate were reacted to yield N2,N4-bis[4-(ethoxycarbonylmethyl)phenyl]-5-trifluoromethyl-2,4-pyrimidinediamine. 1H NMR (CDCl3): δ 8.31 (s, 1H), 7.46 (d, 2H, J=9.0 Hz), 7.45 (d, 2H, J=8.7 Hz), 7.30 (d, 2H, J=9.0 Hz), 7.18 (d, 2H, J=8.7 Hz), 7.16 (bs, 1H), 6.82 (bs, 1H), 4.16 (2q, 4H, J=7.8 Hz), 3.64 (s, 2H), 3.57 (s, 2H), 1.27 (t, 3H, J=7.8 Hz), 1.26 (t, 3H, J=7.8 Hz); 19F NMR (CDCl3): −17223; LCMS: ret. time: 28.07 min.; purity: 99%; MS (m/e): 504 (MH+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08835430B2uspto-grants-2014_09