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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555884Generated: October 26, 2026

Cesium carbonate → HCID 59351199, compound

https://huagongshe.com/reaction/555884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-(Benzo[d]thiazol-2-ylamino)phenolHCID 59326813—
Reactant1-(4-(3-Fluoropyrazin-2-yl)piperidin-1-yl)ethanoneHCID 59351287—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 59351199HCID 59351199—

Reaction Conditions

Temperature80 °C

Reaction Steps

The mixture of 4-(benzo[d]thiazol-2-ylamino)phenol (91 mg, 0.38 mmol), 1-(4-(3-fluoropyrazin-2-yl)piperidin-1-yl)ethanone (56 mg, 0.25 mmol), and cesium carbonate (123 mg, 0.38 mmol) in DMSO (0.85 mL) was heated at 80° C. for 16 h. After cooling to RT, the reaction mixture was partitioned between Teac and brine. The aqueous layer was back extracted with Teac (2×) and the combined organic layer was dried (Na2SO4) and concentrated. The crude material was purified by chromatography through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 0% to 100% Teac in hexane, then 3% MeOH in Teac, followed by reverse-phase preparative HPLC using a Germini C18 5 uM column, 0.1% TFA in CH3CN/H2O, gradient 10% to 100% over 15 min, then neutralize with Si carbonate resin, to provide 1-(4-(3-(4-(benzo[d]thiazol-2-ylamino)phenoxy)pyrazin-2-yl)piperidin-1-yl) as a white solid. MS (ESI, pos. ion) m/z: 445.9 (M+1). IC50 (uM) +++++.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053438B2
Source datasetuspto-grants-2011_11
ORD IDord-87d08f08963248c1b04666ddbb8f3cab
Source noteuspto-grants-2011_11