HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-6-nitroquinazoline → HCID 86698288, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-6-nitroquinazoline | HCID 11356257 | — |
| Reactant | 3-Amino-5-tert-butylselenophene-2-carboxamide | HCID 86646889 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86698288 | HCID 86698288 | 96.5% |
Reaction Steps
To a solution of 4-chloro-6-nitroquinazoline (1.1 g, 5.2 mmol) in isopropanol (10 mL) was added 5-tert-butyl-3-amino-selenophene-2-carboxamide (2.58 g, 10.50 mmol) at rt and the mixture was stirred for 30 min. The mixture was poured into ice cold water and stirred for 15 min The precipitated solid was filtered, washed with water and dried to give the product as a pale yellow color solid (2.1 g, 95%), mp 280-282° C. 1H NMR (400 MHz, DMSO-d6): δ 13.23 (1H, br s), 9.05 (1H, br s), 8.85 (1H, s), 8.56-8.60 (2H, m), 7.98 (1H, d, J=9.2 Hz), 7.80 (2H, br s), 1.43 (9H, s); LC-MS (negative ion mode): m/z 416, 418 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815879B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-dccd8eaaba95447cb7182fb6271cb168 |
| Source note | uspto-grants-2014_08 |