HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Amino-6,7-dimethoxy-2-[4-(2-methylacryloyl)-1-piperazinyl]quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | 2-Piperazine-4-amino-6,7-dimethoxy quinoline hydrochloride | HCID 20473833 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Amino-6,7-dimethoxy-2-[4-(2-methylacryloyl)-1-piperazinyl]quinazoline | HCID 12837098 | 39% |
Reaction Steps
To 20 ml of tetrahydrofuran were added 2.4 g of 4-amino-6,7-dimethoxy-2-(1-piperazinyl)quinazoline hydrochloride and 2.6 g of triethylamine, after which the mixture was stirred for 30 minutes. There was then added 0.6 g of 2-methylacryloyl chloride, after which the mixture was stirred at room temperature for 8 hours. The crystals which were produced were collected by filtration, washed with water and recrystallized from ethanol to give 0.8 g of the desired Compound No. 2 in the form of colourless needles melting at 262°-263° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04426382 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-114bbfd9999b4caeb66de7fe486fa3fe |
| Source note | uspto-grants-1984_01 |