HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-6,7,8-trimethoxyquinazoline → HCID 86698280, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-6,7,8-trimethoxyquinazoline | HCID 100686 | — |
| Reactant | 3-Amino-5-tert-butylselenophene-2-carboxamide | HCID 86646889 | — |
| Reactant | DMF NaOH | HCID 86698281 | — |
| Product | HCID 86698280 | HCID 86698280 | — |
Reaction Steps
The reaction of 4-chloro-6,7,8-trimethoxyquinazoline with 3-amino-5-tert-butylselenophene-2-carboxamide in presence of DMF/NaOH as described in Example 1 gave the title compound as an off-white color solid, mp 218-220° C. 1H NMR (400 MHz, CDCl3): δ 12.08 (1H, br s, exchangeable with D2O), 8.87 (1H, s), 8.78 (1H, s), 7.20 (1H, s), 5.49 (2H, br s, exchangeable with D2O), 4.15 (3H, s), 4.07 (3H, s), 4.06 (3H, s), 1.47 (9H, s); 13C NMR (100 MHz, CDCl3): δ 169.0, 168.6, 154.7, 153.1, 152.6, 147.9, 147.6, 146.6, 142.0, 121.7, 112.0, 109.4, 95.9, 62.1, 61.3, 56.1, 37.2, 32.6; LC-MS (positive ion mode): m/z 463, 465 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815879B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-e88d65de2f3049e19c9b0f6f72230933 |
| Source note | uspto-grants-2014_08 |