HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517269Generated: October 27, 2026
Triethyl Phosphate → 4-(2,5-Dioxo-1-(3-(trifluoromethyl)phenyl)-1,2,3,4,5,6,7,8-octahydroquinazolin-4-yl)-3-(ethylsulfonyl)benzonitrile
https://huagongshe.com/reaction/517269
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl Phosphate | HCID 6535 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | (3-Trifluoromethylphenyl)urea | HCID 25712 | — |
| Reactant | 3-(Ethylsulfonyl)-4-formylbenzonitrile | HCID 58133833 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 4-(2,5-Dioxo-1-(3-(trifluoromethyl)phenyl)-1,2,3,4,5,6,7,8-octahydroquinazolin-4-yl)-3-(ethylsulfonyl)benzonitrile | HCID 86732394 | — |
Reaction Steps
A mixture of triethyl phosphate (4.6 mL, 26.9 mmol) and phosphorous pentoxide (2.54 g, 17.9 mmol) is heated at 50° C. over night and dilutet with tert-butyl methyl ether (45 mL). Cyclohexane-1,3-dione (3.77 g, 33.6 mmol), 3-(ethylsulfonyl)-4-formylbenzonitrile (5.00 g, 22.4 mmol) and 1-(3-(trifluoromethyl)phenyl)urea (4.57 g, 22.4 mmol) are added, and the mixture is heated at reflux for 4 h. The mixture is cooled at room temperature and concentrated under reduced pressure. The residue is purified by reversed phase HPLC (Agilent ZORBAX™ SB-C18, gradient of acetonitrile in water, 0.15% formic acid). Yield: 930 mg; ESI mass spectrum [M+H]+=504; Retention time HPLC: 1.02 min (Z017_S04).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115093B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-b748e31193424503b6b1460c49870459 |
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| Source note | uspto-grants-2015_08 |
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