HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178418806, compound → 3-[[[5-[[4-(3-morpholin-4-ylpropoxy)phenyl]methyl]-1H-pyrazol-3-yl]amino]methylidene]-1H-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Reactant | HCID 178507406 | HCID 178507406 | — |
| Reactant | HCID 178517101 | HCID 178517101 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[[[5-[[4-(3-morpholin-4-ylpropoxy)phenyl]methyl]-1H-pyrazol-3-yl]amino]methylidene]-1H-indol-2-one | HCID 178517076 | — |
Reaction Steps
The named compound is prepared by substituting 5-[4-(3-morpholin-4-yl-propoxy)-benzyl]-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 (0.017 gms.) is reacted with 0.048 gms. of 5-[4-(3-morpholin-4-yl-propoxy)-benzyl]-2H-pyrazol-3-ylamine by refluxing in tetrahydrofuran (1.0 mL). Recrystallization from a mixture of ethyl acetate and hexanes affords the named compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07005444B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-f5f2f5e6b26f46af96f6da425a9656d2 |
| Source note | uspto-grants-2006_02 |