HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 2-[N-(3-Ethoxycarbonylpropyl)-N-methylamino]-4-(3,4-methylenedioxybenzyl)amino-6-cyanoquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-(methylamino)butanoate hydrochloride | HCID 14177893 | — |
| Reactant | 2-Chloro-4-(3,4-methylenedioxybenzyl)amino-6-cyanoquinazoline | HCID 21183984 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[N-(3-Ethoxycarbonylpropyl)-N-methylamino]-4-(3,4-methylenedioxybenzyl)amino-6-cyanoquinazoline | HCID 22069343 | 77.6% |
Reaction Steps
858 mg of ethyl N-methyl-4-aminobutyrate hydrochloride, 238 mg of triethylamine, 4 ml of 2-propanol and 2 ml of N,N-dimethylformamide were added to 400 mg of 2-chloro-4-(3,4-methylenedioxybenzyl)amino-6-cyanoquinazoline. The obtained mixture was refluxed for 1 hour, cooled to room temperature and filtered. The filtrate was distilled under a reduced pressure to remove the solvent and the residue was recrystallized (from ethanol/water) to give 410 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576322 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-490a2394c98145c2addf02dcc5ca8f84 |
| Source note | uspto-grants-1996_11 |