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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972741Generated: November 1, 2026

1,3-Dibromo-5,5-dimethylhydantoin → HCID 58529949, compound

https://huagongshe.com/reaction/1972741

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantHCID 58529978HCID 58529978—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 58529949HCID 58529949109.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (−20° C.) solution of tert-butyl 4-[4-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-1,3-thiazol-2-yl]piperidine-1-carboxylate (914 mg. 2.28 mmol) in DMF (12.6 mL) and AcOH (5 mL) was added 1,3-dibromo-5,5-dimethylhydantoin (326 mg, 1.14 mmol) in 3 portions over 10 minutes. The mixture was stirred at 0° C. for 3 h. The reaction was quenched with the addition 5% aqueous K2CO3 (50 mL) and was allowed to warm to rt. The mixture was extracted with ethyl acetate (3×50 mL). The combined organics were washed with brine, dried (Na2SO4) and evaporated. The crude material was purified by ISCO® chromatography using a gradient of 50% to 75% ethyl acetate in hexanes to afford 596 mg (54%) of the desired product. ES-MS m/z 480.85 [M+H]+, HPLC RT (min) 3.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-7309a98d23c14e82bee54a90bba21eb2
Source noteuspto-grants-2013_04