HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 12837102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Pentenoyl chloride | HCID 4228493 | — |
| Reactant | 2-Piperazine-4-amino-6,7-dimethoxy quinoline hydrochloride | HCID 20473833 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 12837102 | HCID 12837102 | 41.7% |
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 20 minutes. There was then added 0.78 g of 4-pentenoyl chloride, after which the mixture was stirred at room temperature for 15 hours. The resulting crystals were collected by filtration, washed with water and recrystallized from ethanol, to give 1.02 g of the desired Compound No. 6 in the form of pale brown needles melting at 219°-220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04426382 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-de6201d379fd422882dfa259b537e488 |
| Source note | uspto-grants-1984_01 |