HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(furan-2-yl)-1H-pyrazol-5-amine → HCID 178517183, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(furan-2-yl)-1H-pyrazol-5-amine | HCID 523183 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Reactant | HCID 178517101 | HCID 178517101 | — |
| Reactant | (3Z)-5-fluoro-3-(hydroxymethylidene)-1H-indol-2-one | HCID 178517185 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178517183 | HCID 178517183 | — |
Reaction Steps
The named compound is prepared by substituting E & Z-3-[(hydroxy)-methylene]-5-fluoro-1,3-dihydro-indol-2-one for E & Z-3-[(hydroxy)-methylene]-1,3-dihydro-indol-2-one and 3-amino-5-(2-furyl)-pyrazole for 3-aminopyrazole in the reaction of Example 1. Specifically, E & Z-3-[(hydroxy)-methylene]-5-fluoro-1,3-dihydro-indol-2-one (0.050 gms.) is reacted with 0.085 gms. of 3-amino-5-(2-furyl)-pyrazole by refluxing in tetrahydrofuran (1.5 mL).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07005444B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-e9bbdaaf1d5a4230bae43e17985f2521 |
| Source note | uspto-grants-2006_02 |