HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Chloro-n-(5-methyl-1h-pyrazol-3-yl)quinazolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| 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-dichloroquinazoline (12.69 g, 63 mmol) and 3-amino-5-methylpyrazole (6.18 g, 63 mmol) in ethanol (220 mL) is added triethylamine (8.13 mL, 63 mmol) and the reaction mixture is stirred for 3 hours at room temperature. The pale yellow precipitate is then collected by filtration, washed with cold ethanol and dried under vacuum to give (2-chloroquinazolin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087603B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-40d7272e26be49c1ab66795f224e7323 |
| Source note | uspto-grants-2006_08 |