HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73677Generated: October 28, 2026
1,3-Dibromo-5,5-dimethylhydantoin → HCID 57955300, compound
https://huagongshe.com/reaction/73677
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | HCID 57758195 | HCID 57758195 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57955300 | HCID 57955300 | 107% |
Reaction Steps
To a solution of THF (500 mL) was added 1-{4-[4-amino-6-(methoxymethyl)pyrrolo[2,1-f][1,2,4]triazin-5-yl]-2-fluorophenyl}-3-[2-fluoro-5-(trifluoromethyl)phenyl]urea (2.29 g, 4.65 mmol). The solution was cooled to −40° C. and then 1,3-dibromo-5,5-dimethylhydantoin (665 mg, 2.33 mmol) was added in two batches 20 min apart. The reaction was stirred at −40° C. for 1 h and then allowed to warm to rt over the following 2 h. Aq saturated Na2SO3 was added to the reaction followed by EtOAc. The layers were separated and the aqueous layer was back extracted with EtOAc. The organic layer was washed with 1 N NaOH and water, dried (Na2SO4), filtered and evaporated to yield 2.83 g crude (107%) of the desired product. MS [M+H]+=571; LCMS RT=3.54.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829185B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-48137c0dc47a498eb3bcfda5df59c03b |
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| Source note | uspto-grants-2014_09 |
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