HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 4(1H)-Quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Quinazolinedione | HCID 64048 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Dibenzylphosphite | HCID 21904359 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4(1H)-Quinazolinone | HCID 135408753 | 185.4% |
Reaction Steps
The quinazoline 1 (0.2 g, 0.62 mmol) was dissolved in CH3CN (5 mL). After cooling to −10° C. (ice/NaCl), CCl4, DIEA and DMAP were added. After stirring for 10 min, a solution of dibenzyl phosphite in CH3CN (2 mL) was slowly added over 10 min. Stirring was continued at −10° C. for 2 h, then at RT for 24 h. Quenched by addition of 0.5 M K2HPO4, diluted with water (15 mL), extracted with DCM (30 mL), dried, concentrated, purified by flash chromatography (100% DCM) to obtain 2 (168 mg, 47% yield) as a colorless oil. LC/MS (10-99%) M/Z 586.0 retention time 2.54 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153642B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-c6bc495d3f8e4c618a55de48b09d748a |
| Source note | uspto-grants-2012_04 |