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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435317Generated: November 3, 2026

Potassium Iodide → HCID 58777653, compound

https://huagongshe.com/reaction/1435317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 10414333HCID 10414333—
SolventWaterHCID 962—
SolventSodium ChlorideHCID 5234—
SolventDimethylformamideHCID 6228—
ProductHCID 58777653HCID 5877765351.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

A suspension of [4-amino-2-[1-(3-chloro-propane-1-sulfonyl)-piperidin-4-ylamino]-pyrimidin-5-yl]-(5-fluoro-2-methoxy-phenyl)-methanone (80 mg, 0.16 mmol, Example 273), potassium iodide (100 mg, 0.61 mmol), and potassium acetate (120 mg, 1.22 mmol) in dimethylformamide (6 mL) was heated at 65-85° C. under nitrogen for 14 hours. The resulting solution was diluted with 50 mL of cold water plus 20 mL of saturated aqueous sodium chloride. Solids were filtered, collected and dissolved in methylene chloride. After washing with water, the organic layer was separated and dried (Na2SO4). The residue was purified by silica gel chromatography (ethyl acetate/hexane) and crystallized from methylene chloride/ethyl ether to give acetic acid 3-[4-[4-amino-5-(5-fluoro-2-methoxy-benzoyl)-pyrimidin-2-ylamino]-piperidine-1-sulfonyl]-propyl ester as a white solid (42 mg, 51% yield). HRMS, observed: 510.1822; Calcd for (M+H)+: 510.1817

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615634B2
Source datasetuspto-grants-2009_11
ORD IDord-d4361227662d403ab0961cffc9daacd9
Source noteuspto-grants-2009_11