Triethylamine → 2-(4-{3-[2-(4-Chloro-phenyl)-2H-indazol-3-yl]-3-cyclohexyl-ureido}-3-fluoro-phenyl)-2-methyl-propionic acid methyl ester
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:16]([NH:17][CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[C:15]3[C:10]([CH:11]=[CH:12][CH:13]=[CH:14]3)=[N:9]2)=[CH:4][CH:3]=1.[CH3:24][O:25][C:26](=[O:40])[C:27]([C:30]1[CH:35]=[CH:34][C:33]([N:36]=[C:37]=[O:38])=[C:32]([F:39])[CH:31]=1)([CH3:29])[CH3:28].CCN(CC)CC>ClCCCl>[CH3:24][O:25][C:26](=[O:40])[C:27]([C:30]1[CH:35]=[CH:34][C:33]([NH:36][C:37]([N:17]([C:16]2[N:8]([C:5]3[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=3)[N:9]=[C:10]3[C:15]=2[CH:14]=[CH:13][CH:12]=[CH:11]3)[CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)=[O:38])=[C:32]([F:39])[CH:31]=1)([CH3:29])[CH3:28]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In analogy to the procedure described in example 1.2, [2-(4-chloro-phenyl)-2H-indazol-3-yl]-cyclohexyl-amine (example 9.1) was reacted with 2-(3-fluoro-4-isocyanato-phenyl)-2-methyl-propionic acid methyl ester in 1,2-dichloroethane in the presence of Et3N for 3 days under reflux conditions to give the title compound as yellow solid. MS: m/e=563.5 [M+H+].
Sources & evidence
- ORD record
- ord-644b31ec186a4f92b275c4a4c0c9b7a1
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08153663B2
Reaction notes
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