HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-chloro-N-(2,5-dimethoxyphenyl)-N-methylquinazolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-Chloro-N-(2,5-dimethoxyphenyl)quinazolin-4-amine | HCID 22692737 | — |
| Product | 2-chloro-N-(2,5-dimethoxyphenyl)-N-methylquinazolin-4-amine | HCID 11255967 | — |
Reaction Steps
The title compound was prepared from (2-chloro-quinazolin-4-yl)-(2,5-dimethoxy-phenyl)-amine and methyl iodide by a procedure similar to Example 36 (78% yield). 1H NMR (CDCl3): 7.72-7.75 (m, 1H), 7.56 (ddd, J=8.4, 5.7 and 2.1 Hz, 1H), 6.98-7.00 (m, 2H), 6.92-6.92 (m, 2H), 6.78-6.79 (m, 1H), 3.75 (s, 3H), 3,58 (s, 3H), 3.56 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309562B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-ce2eb36a6fb74009835bd00e1eddfd49 |
| Source note | uspto-grants-2012_11 |