HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → N-(4-(4-(3-methyl-1H-pyrazol-5-ylamino)quinazolin-2-ylthio)phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-Mercaptoacetanilide | HCID 70777 | — |
| Reactant | 2-Chloro-n-(5-methyl-1h-pyrazol-3-yl)quinazolin-4-amine | HCID 21939163 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | N-(4-(4-(3-methyl-1H-pyrazol-5-ylamino)quinazolin-2-ylthio)phenyl)acetamide | HCID 178419068 | — |
Reaction Steps
A solution of (2-chloroquinazolin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine (200 mg, 0.77 mmol) and 4-acetamidothiophenol (644 mg, 3.85 mmol) is refluxed in tert-butanol (3 mL) over a 20 hour period. Diethylether (10 mL) is added to the mixture and a solid forms that is collected by filtration. This solid is suspended in EtOH/H2O 1 mL/3 mL), then K2CO3 (110 mg, 0.8 mmol) is added and the suspension is stirred for 2 h at room temperature. A solid forms and is collected and dried under vacuum to give the product [2-(4-acetamidophenylsulfanyl)-quinazolin-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-6aa0dda9a02f442b9c2c4c5c4181c787 |
| Source note | uspto-grants-2006_08 |