HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-Amino-2-chloro-5-cyclobutyloxy-6,7-dimethoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 5-Cyclobutyloxy-2,4-dichloro-6,7-dimethoxyquinazoline | HCID 18470642 | — |
| Product | 4-Amino-2-chloro-5-cyclobutyloxy-6,7-dimethoxyquinazoline | HCID 18470657 | 68% |
Reaction Steps
5-Cyclobutyloxy-2,4-dichloro-6,7-dimethoxyquinazoline (300 mg, 0.0009 mol) was suspended in a saturated ethanolic ammonia solution (10 ml) and the reaction stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, resuspended in a minimum volume of diethyl ether and the resulting solid filtered off. Drying under suction gave the subtitle compound as a white solid (189 mg, 68%). Rf 0.69 (diethyl ether). 1H-NMR (CDCl3): δ=1.56 (1H, m), 1.82 (1H, m), 2.26 (2H, m), 2.42 (2H, m), 3.85 (3H, s), 3.94 (3H, s), 4.92 (1H, m), 5.82 (1H, bs), 6.94 (1H, s), 7.72 (1H, bs).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048864 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-aec7425699ff4ece9802af7a3af6e204 |
| Source note | uspto-grants-2000_04 |