HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069208Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 11539494, compound
https://huagongshe.com/reaction/2069208
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-(6-fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide | HCID 58964482 | — |
| Reactant | HCID 178418822 | HCID 178418822 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11539494 | HCID 11539494 | 77% |
Reaction Steps
A mixture of 50 mg (0.156 mmol) of N-(6-fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide, 139 mg (0.936 mmol) of 4-phenyl-1H-imidazole and 0.25 ml of DMSO is heated to 120° C. for 3.5 hours. After cooling to room temperature, the reaction mixture is distributed between ethyl acetate and water, the organic phase is separated, washed with water and brine, dried over sodium sulfate, filtered and evaporated. The residue is chromatographed on silica gel using tetrahydrofuran-hexane (80:20) and the fractions containing the desired product are combined and evaporated giving 53 mg (77%) of the title compound. MS (ES−): m/e=441 (M−1−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08299085B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-110f7cb3996749f88e8fdc817dccb506 |
|---|
| Source note | uspto-grants-2012_10 |
|---|