HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Pyrazol-3-amine, 5-methyl- → 2-Chloro-n-(5-methyl-1h-pyrazol-3-yl)quinazolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Pyrazol-3-amine, 5-methyl- | HCID 93146 | — |
| Reactant | 2,4-Dichloroquinazoline | HCID 252886 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Chloro-n-(5-methyl-1h-pyrazol-3-yl)quinazolin-4-amine | HCID 21939163 | — |
Reaction Steps
To a solution of 2,4-dichloro-quinazoline (3.3 g, 16.6 mmol) in anhydrous ethanol (150 mL) is added 5-methyl-1H-pyrazol-3-yl amine (3.2 g, 32.9 mmol). The mixture is stirred at room temperature for 4 h, and the resulting precipitate is collected by filtration, washed with ethanol, and dried under vacuum to afford (2-chloro-quinazolin-4-yl)-(5-methyl-1H-pyrazol-3-yl)-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07098330B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-9b8e8ee433ae4003923410d0cc30e418 |
| Source note | uspto-grants-2006_08 |