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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037006Generated: October 30, 2026

3-Chlorophenol → HCID 178518505, compound

https://huagongshe.com/reaction/2037006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorophenolHCID 7933—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178504622HCID 178504622—
ReactantHCID 178504850HCID 178504850—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178518505HCID 17851850569%

Reaction Conditions

Temperature90 °C

Reaction Steps

A (1:1) mixture of (Z)-5-((4-(cyclopropylamino)-2-(methylsulfonyl)pyrazolo[1,5-a][1,3,5]triazin-8-yl)methylene)imidazolidine-2,4-dione and (Z)-5-((4-(cyclopropylamino)-2-(methylsulfinyl)pyrazolo[1,5-a][1,3,5]triazin-8-yl)methylene)imidazolidine-2,4-dione (1.0 eq, 25 mg, 0.0704 mmol) was combined in a vial with 3-chlorophenol (5.0 eq, 45 mg, 0.35 mmol) and K2CO3 (5.0 eq, 48 mg, 0.347 mmol) in NMP (0.2 ml). The mixture was stirred at 90° C. for 1 hour. Water was added and the resulting solid was filtered and dried. Trituration in a mixture of ethyl acetate and hexanes followed by filtration provided (Z)-5-((2-(3-chlorophenoxy)-4-(cyclopropylamino)pyrazolo[1,5-a][1,3,5]triazin-8-yl)methylene)imidazolidine-2,4-dione as a tan solid (20 mg, 69%). LCMS (ES):>95% pure, m/z 412 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575177B2
Source datasetuspto-grants-2013_11
ORD IDord-80ec8da7f0b1487bbf77ad8a56652de2
Source noteuspto-grants-2013_11