Diisopropylethylamine → HCID 57755856, compound

HRID 227738Notes

Reaction equation

HRID 227738 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:9]2[C:14]([C:15]([OH:17])=O)=[C:13]([CH3:18])[NH:12][C:11](=[O:19])[NH:10]2)[CH:5]=[C:6]([F:8])[CH:7]=1.[F:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]2[C:35]3[C:30](=[CH:31][CH:32]=[C:33]([NH2:36])[CH:34]=3)[NH:29][N:28]=2)=[CH:23][CH:22]=1.C1CN([P+](Br)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C>C(Cl)Cl>[F:20][C:21]1[CH:22]=[CH:23][C:24]([C:27]2[C:35]3[C:30](=[CH:31][CH:32]=[C:33]([NH:36][C:15]([C:14]4[CH:9]([C:4]5[CH:5]=[C:6]([F:8])[CH:7]=[C:2]([F:1])[CH:3]=5)[NH:10][C:11](=[O:19])[NH:12][C:13]=4[CH3:18])=[O:17])[CH:34]=3)[NH:29][N:28]=2)=[CH:25][CH:26]=1

Participants

6

Reactant 4

HCID 81531DiisopropylethylamineHCID 2733179PyBroPHCID 224802843-(4-fluorophenyl)-1H-indazol-5-amineHCID 57755878HCID 57755878, compound

Product 1

HCID 57755856HCID 57755856, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The titled compound was prepared following the procedure of Example 175 using 4-(3,5-Difluoro-phenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid, 3-(4-Fluoro-phenyl)-1H-indazole-5-ylamine, PyBroP and diisopropylethylamine in methylene chloride. MS (ESI) m/z=478 [M+H]+.

Sources & evidence

ORD record
ord-b8cc0519729141bd89703aba45291d67
Source dataset
uspto-grants-2009_07
Patent number
US07560467B2

Reaction notes

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