HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloro-6-methylquinazoline → N-(3-Aminooxetan-3-ylmethyl)-2-chloro-6-methylquinazolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloro-6-methylquinazoline | HCID 14256483 | — |
| Reactant | 3-(Aminomethyl)oxetan-3-amine | HCID 21713016 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3-Aminooxetan-3-ylmethyl)-2-chloro-6-methylquinazolin-4-amine | HCID 86691401 | — |
Reaction Steps
A solution of 2,4-dichloro-6-methylquinazoline (645 mg, 3 mmol) and 3-(aminomethyl)oxetan-3-amine (340 mg, 3.3 mmol) in methanol (15 mL) was stirred at room temperature overnight. After the resulting mixture was concentrated in vacuo, the residue was purified by column chromatography (eluting with 10% methanol in dichloromethane) to afford the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871756B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-463f9b1bff4f4f8cb51f8be1b520ec80 |
| Source note | uspto-grants-2014_10 |