HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → 2-Allylamino-4-isopropylamino-6-nitroquinazoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | 2-Chloro-4-isopropylamino-6-nitroquinazoline | HCID 18326428 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Allylamino-4-isopropylamino-6-nitroquinazoline hydrochloride | HCID 18326501 | — |
Reaction Steps
To 870 mg (3.26 mmol) of 2-chloro-4-isopropylamino-6-nitroquinazoline was added 3.81 g (66.64 mmol) of allylamine, followed by stirring at room temperature for 4 hours. To the reaction solution was added water, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 895 mg (yield: 95.7%) of a free base compound of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06339089B2 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-3452785b83ad483896bc3e4eef052c71 |
| Source note | uspto-grants-2002_01 |