HCID 14722178, compound → HCID 10039959, compound
Reaction equation
C([O:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([NH:11][C:12]2[N:17]=[C:16]([C:18]3[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=3)[CH:15]=[CH:14][N:13]=2)[CH:6]=1)C.C(OC(=O)C1C=CC(C)=C(NC2N=C(C3C=NC=CC=3)C=CN=2)C=1)C>>[N:20]1[CH:21]=[CH:22][CH:23]=[C:18]([C:16]2[CH:15]=[CH:14][N:13]=[C:12]([NH:11][C:7]3[CH:6]=[C:5]([CH:10]=[CH:9][CH:8]=3)[C:4]([OH:24])=[O:3])[N:17]=2)[CH:19]=1Participants
3
Procedure
Utilising the procedure described in example 1c but employing 3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-benzoic acid ethyl ester in lieu of 4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-benzoic acid ethyl ester, afforded the title compound as a crystalline solid, m.p. 291-295° C.
Sources & evidence
- ORD record
- ord-aea4037095964ce0a5451d06c0c6d7d8
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07569566B2
Reaction notes
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