1-Ethyl-1H-pyrazol-5-amine → HCID 178463040, compound
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.[CH2:19]([N:21]1[C:25]([NH2:26])=[CH:24][CH:23]=[N:22]1)[CH3:20]>O1CCCC1>[CH2:19]([N:21]1[C:25]([NH:26][CH:8]=[C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][C:10]2=[O:18])=[CH:24][CH:23]=[N:22]1)[CH3:20]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The named compound is prepared by substituting 2-ethyl-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 0.1632 gms. 2-ethyl-2H-pyrazol-3-ylamine by refluxing in tetrahydrofuran (2.5 mL).
Workup
- customThe named compound is prepared
- customin the reaction of Example 1
Sources & evidence
- ORD record
- ord-7f8b8e464e5d492ca25512840b95fd55
- Source dataset
- uspto-grants-2006_02
- Patent number
- US07005444B2
Reaction notes
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