HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroquinazoline → 4-Quinazolinamine, N-[2-(2-naphthalenyl)ethyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroquinazoline | HCID 78864 | — |
| Reactant | 2-(2-Naphthyl)ethyl-amine | HCID 3784378 | — |
| Reactant | Water ammonium hydroxide | HCID 86589665 | — |
| Product | 4-Quinazolinamine, N-[2-(2-naphthalenyl)ethyl]- | HCID 164161 | 26.7% |
Reaction Steps
A mixture of 1.0 g of 4-chloroquinazoline and 2.0 g of 2-(2-naphthyl)ethyl amine was heated under nitrogen to 165°-170° C. for one hour. The mixture was cooled and then 200 ml of a 50/50 mixture of ammonium hydroxide/water was added. The product was extracted into CH2Cl2, and the resulting solution was treated with charcoal and filtered. The solution was then concentrated to dryness, and the residue was recrystallized from a mixture of pentane and CH2Cl2 to give: 0.480 g of the title product. Yield: 26.7%. M.P. 172°-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05411963 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-39812333389f4f1ba1923e4b17188cbd |
| Source note | uspto-grants-1995_05 |