Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium SulfiteHCID 24437—
ReactantHCID 57758195HCID 57758195—
SolventEthyl AcetateHCID 8857—
ProductHCID 57955300HCID 57955300107%

Reaction Conditions

Temperature-40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829185B2
Source datasetuspto-grants-2014_09
ORD IDord-48137c0dc47a498eb3bcfda5df59c03b
Source noteuspto-grants-2014_09