HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-(3-Ethoxycarbonylpropyl)Amino-6,7,8-Trimethoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-6,7,8-trimethoxyquinazoline | HCID 100686 | — |
| Reactant | 4-Aminobutyrate ethyl hydrochloride | HCID 12649661 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(3-Ethoxycarbonylpropyl)Amino-6,7,8-Trimethoxyquinazoline | HCID 9798450 | 72% |
Reaction Steps
1.0 g of ethyl 4-aminobutyrate hydrochloride (6.0 mmol), 2 ml of triethylamine, 10 ml of tetrahydrofuran and 10 ml of 2-propanol are added to 0.50 g (2.0 mmol) of 4-chloro-6,7,8-trimethoxyquinazoline, followed by heating under reflux one whole day and night. The reaction liquid is distilled under reduced pressure to remove the solvent. The obtained residue is purified by silica gel column chromatography (ethyl acetate) and then recrystallized from ethyl acetate/hexane. Thus, 0.49 g (yield 72%) of a white crystal is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990117 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-f89c6bd37f1e46618a85f45d67f39c63 |
| Source note | uspto-grants-1999_11 |