HCID 178418806, compound → HCID 178423869, compound

HRID 892039Notes

Reaction equation

HRID 892039 reaction equation
NC1C=CNN=1.O/[CH:8]=[C:9]1\[C:10](=[O:18])[NH:11][C:12]2[C:17]\1=[CH:16][CH:15]=[CH:14][CH:13]=2.[CH3:19][C:20]1[CH:25]=[C:24]([CH3:26])[N:23]=[C:22]2[NH:27][N:28]=[C:29]([NH2:30])[C:21]=12>O1CCCC1>[CH3:19][C:20]1[CH:25]=[C:24]([CH3:26])[N:23]=[C:22]2[NH:27][N:28]=[C:29]([NH:30][CH:8]=[C:9]3[C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[NH:11][C:10]3=[O:18])[C:21]=12

Participants

5

Reactant 3

HCID 178418806HCID 178418806, compoundHCID 178423895HCID 178423895, compoundHCID 178517101HCID 178517101, compound

Product 1

HCID 178423869HCID 178423869, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

The named compound is prepared by substituting 4,6-dimethyl-1H-pyrazolo[3,4-b]pyridin-3-ylamine for 3-aminopyrazole in the reaction of Example 1. Specifically, E & Z-3-[(hydroxy)-methylene]-1,3-dihydro-indol-2-one (0.100 gms.) is reacted with 0.2118 gms. of 4,6-dimethyl-1H-pyrazolo[3,4-b]pyridin-3-ylamine by refluxing in tetrahydrofuran (2.5 mL).

Workup

  1. customThe named compound is prepared
  2. customin the reaction of Example 1

Sources & evidence

ORD record
ord-be4ffbae9c854da9931132636f7f6c47
Source dataset
uspto-grants-2006_02
Patent number
US07005444B2

Reaction notes

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