HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 46840742, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | HCID 70876732 | HCID 70876732 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46840742 | HCID 46840742 | — |
Reaction Steps
To a solution of 3-(4-sec-butyl-phenyl)-7-fluoro-2-[4-(2-hydroxy-ethoxy)-3,5-dimethyl-phenyl]-2,3-dihydro-1H-quinazolin-4-one (0.11 g, 0.24 mmol) in anhydrous THF (30 mL) was added DDQ (0.09 g, 0.4 mmol) and the reaction mixture was stirred for 72 hours at room temperature. The solvent was evaporated in vacuo and the crude material was purified by column chromatography (silica gel; 230-400 mesh; 0.5% methanol/CH2Cl2 as eluent) to give the title compound (Q) as white solid. Yield: 0.06 g (50%). MP 53.9-54.4° C. 1H-NMR (400 MHz, CDCl3): δ 8.38 (dd, 1H), 7.43 (dd, 1H), 7.22-7.05 (m, 5H), 6.99 (s, 2H), 3.90 (m, 2H), 3.78 (m, 2H), 2.59 (m, 1H), 2.16 (s, 6H), 2.05 (t, 1H), 1.59 (m, 2H), 1.20 (d, 3H), 0.71 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952021B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-cd7ac15ea5bd40d2ab4a7f7d0d6e3386 |
| Source note | uspto-grants-2015_02 |