HCID 178418806, compound → HCID 178489752, compound

HRID 411697Notes

Reaction equation

HRID 411697 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][O:20][C:21]1[CH:22]=[C:23]([C:27]2[CH:28]=[C:29]([NH2:32])[NH:30][N:31]=2)[CH:24]=[CH:25][CH:26]=1>O1CCCC1>[CH3:19][O:20][C:21]1[CH:22]=[C:23]([C:27]2[CH:28]=[C:29]([NH:32][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])[NH:30][N:31]=2)[CH:24]=[CH:25][CH:26]=1

Participants

5

Reactant 3

HCID 178418806HCID 178418806, compoundHCID 178489814HCID 178489814, compoundHCID 178517101HCID 178517101, compound

Product 1

HCID 178489752HCID 178489752, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

The named compound is prepared by substituting 5-(3-methoxy-phenyl)-2H-pyrazol-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 0.2367 gms. 5-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine by refluxing in tetrahydrofuran (2.0 mL) over the weekend.

Workup

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

Sources & evidence

ORD record
ord-846bbb694a764f0ea942560daf6d0992
Source dataset
uspto-grants-2003_05
Patent number
US06559173B1

Reaction notes

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