HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244811Generated: November 1, 2026
Potassium Carbonate → 2-(6-quinazolinoxy)-N-(4-methylpent-2-yn-4-yl) butyramide
https://huagongshe.com/reaction/1244811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Quinazolin-6-ol | HCID 589643 | — |
| Reactant | 2-bromo-N-(4-methylpent-2-yn-4-yl)butyramide | HCID 21078406 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(6-quinazolinoxy)-N-(4-methylpent-2-yn-4-yl) butyramide | HCID 69254970 | 93.9% |
Reaction Steps
6-Hydroxyquinazoline (0.060 g, prepared as described in J. Chem. Soc. (1952), 4985) and 2-bromo-N-(4-methylpent-2-yn-4-yl) butyramide (0.101 g) were dissolved in dry N,N-dimethylformamide (2 ml) containing anhydrous potassium carbonate (0.088 g). The mixture was stirred and heated to 80° C. for 5 hours then allowed to cool to ambient temperature and stored for 18 hours. The brown suspension was diluted with water, extracted into ethyl acetate and the organic phase separated, washed with water, dried over magnesium sulphate and evaporated under reduced pressure to give a pale brown oil. The oil was fractionated by chromatography (silica; ethyl acetate/hexane, 4:1 by volume) to give the title product (0.12 g) as a pale brown gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07122672B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-0577450bb10c46ae8d4107c21ed17d1c |
|---|
| Source note | uspto-grants-2006_10 |
|---|