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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994023Generated: October 31, 2026

Methanol → HCID 178503502, compound

https://huagongshe.com/reaction/1994023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCesium carbonateHCID 10796—
Reactant4-Amino-6-chloro-2-methylthiopyrimidineHCID 70496—
ReactantHCID 178515914HCID 178515914—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178503502HCID 17850350227.7%

Reaction Steps

4-(5-{[3-(trifluromethyl)phenyl]amino}-4H-1,2,4-triazol-3-yl)phenol (100 mg, 0.31 mmol) was dissolved in 3 mL of anhydrous dioxane in 2-5 mL microwave vial (Personal Chemistry). Solid Cs2CO3 (101.7 mg, 0.31 mmol) was added, followed by 4-amino-6-chloro-2-(methylthio)-pyrimidine (60.3 mg, 0.34 mmol). The vial was capped and microwaved at 200° C. for 10 min. Then ca. 3 mL of MeOH was added to dissolve the formed suspension. The resulting reddish-brown solution was transferred into a round-bottom flask and solvent was removed in vacuo. The residue was re-dissolved in 3 mL of DMF, filtered through 0.22 u syringe filter and purified by reverse phase preparative HPLC using acetontrile/water system with 0.01% of TFA. The fractions, containing the product, were collected and partitioned between EtOAc and saturated aqueous NaHCO3. Ethyl acetate layer was washed with brine, dried over anhydrous sodium sulfate and filtered. Solvent was removed in vacuo to give the title compound as a white solid (39.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-c3f08f88bc4e4a1e8a7e3a9b0963da80
Source noteuspto-grants-2010_01