HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → 4-(1-Adamantylamino)-2-allylamino-6-nitroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | 4-(1-Adamantylamino)-2-chloro-6-nitroquinazoline | HCID 18326433 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(1-Adamantylamino)-2-allylamino-6-nitroquinazoline | HCID 18326520 | 88.7% |
Reaction Steps
To 82 mg (0.25 mmol) of 4-(1-adamantylamino)-2-chloro-6-nitroquinazoline was added 1.00 ml (13.33 mmol) of allylamine, and the resulting mixture was stirred at room temperature overnight. 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 77 mg (88.7%) 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-c054063fe66648fda753fc91b724e657 |
| Source note | uspto-grants-2002_01 |