HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069207Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 11539559, compound
https://huagongshe.com/reaction/2069207
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 178418934 | HCID 178418934 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11539559 | HCID 11539559 | 21.7% |
Reaction Steps
A mixture of 20 mg (0.062 mmol) of N-(6-fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide, 56 mg (0.372 mmol) of 4-bromo-1H-imidazole and 0.1 ml of DMSO is heated to 120° C. for 16 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 dichloro-methane-methanol (95:5) and the fractions containing the desired product are combined and evaporated yielding 6 mg (21%) of the title compound. MS (ES−): m/e=445 (M−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299085B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-558dd220fe12477c9de3428e8f0dd92a |
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| Source note | uspto-grants-2012_10 |
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