HCID 68827536, compound → HCID 178429242, compound

HRID 734725Notes

Reaction equation

HRID 734725 reaction equation
[CH3:1][N:2]1[C:7](=[O:8])[CH2:6][CH:5]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=2)[C:4]([C:19]([OH:21])=O)=[C:3]1[CH3:22].[NH2:23][C:24]1[CH:25]=[C:26]2[C:30](=[CH:31][CH:32]=1)[NH:29][N:28]=[C:27]2[Cl:33]>>[Cl:33][C:27]1[C:26]2[C:30](=[CH:31][CH:32]=[C:24]([NH:23][C:19]([C:4]3[CH:5]([C:9]4[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:16])[F:17])=[CH:11][CH:10]=4)[CH2:6][C:7](=[O:8])[N:2]([CH3:1])[C:3]=3[CH3:22])=[O:21])[CH:25]=2)[NH:29][N:28]=1

Participants

3

Reactant 2

HCID 68827536HCID 68827536, compoundHCID 178507360HCID 178507360, compound

Product 1

HCID 178429242HCID 178429242, compound

Procedure

The title compound was prepared from the product of Example 41, Step 2 and 5-amino-3-chloroindazole using the method described in Example 56, Step 3. MS (ES+) m/e 463 [M+H]+

Sources & evidence

ORD record
ord-b085cc9017114ca6a8b807778e43df73
Source dataset
uspto-grants-2009_09
Patent number
US07592357B2

Reaction notes

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