HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-6,7-dimethoxy-2-methylquinazoline → HCID 86698302, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-6,7-dimethoxy-2-methylquinazoline | HCID 10490150 | — |
| Reactant | HCID 86646889 | HCID 86646889 | — |
| Reactant | HCID 86698281 | HCID 86698281 | — |
| Product | HCID 86698302 | HCID 86698302 | — |
Reaction Steps
The reaction of 4-chloro-6,7-dimethoxy-2-methylquinazoline with 3-amino-5-tert-butylselenophene-2-carboxamide in the presence of DMF/NaOH as described in Example 1 gave title compound as an off-white color solid, mp 266-268° C. 1H NMR (400 MHz, CDCl3): δ 11.95 (1H, br s, exchangeable with D2O), 8.97 (1H, s), 7.32 (1H, s), 7.19 (1H, s), 5.38 (2H, br s, exchangeable with D2O), 4.08 (3H, s), 4.01 (3H, s), 2.70 (3H, s), 1.47 (9H, s); 13C NMR (100 MHz, CDCl3): δ 168.63, 168.60, 162.1, 154.8, 154.5, 149.2, 148.2, 148.1, 121.9, 109.0, 107.4, 107.1, 100.1, 56.2, 56.1, 37.1, 32.5, 26.3; LC-MS (negative ion mode): m/z 445, 447 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815879B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-a5ce7105f4f74c7c9a9369bfee1aa132 |
| Source note | uspto-grants-2014_08 |