HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(3-Carboxypropyl)Amino-6,7,8-Trimethoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(3-Ethoxycarbonylpropyl)Amino-6,7,8-Trimethoxyquinazoline | HCID 9798450 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(3-Carboxypropyl)Amino-6,7,8-Trimethoxyquinazoline | HCID 9861907 | 744% |
Reaction Steps
5 ml of a 1N aqueous solution of sodium hydroxide is added to a solution of 0.52 g (1.5 mmol) of the 4-(3-ethoxycarbonylpropyl)amino-6,7,8-trimethoxyquinazoline obtained in Example 1 in tetrahydrofuran (5 ml)/ethanol (5 ml), followed by stirring at room temperature one whole day and night. The reaction liquid is neutralized with 5 ml of 1N hydrochloric acid, and then concentrated under reduced pressure. The crystals thus precipitated are recovered by filtration, washed with water, and dried with air. Thus, 0.36 g (yield 744%) of a pale-yellow crystal is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990117 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-0a80c348d3af4ddcb017380d41b1652c |
| Source note | uspto-grants-1999_11 |