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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048722Generated: October 30, 2026

Sodium Chloride → HCID 90032105, compound

https://huagongshe.com/reaction/1048722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantCesium carbonateHCID 10796—
ReactantN-(3-hydroxyphenyl)methanesulfonamideHCID 836758—
ReactantHCID 90031616HCID 90031616—
SolventDimethylformamideHCID 6228—
ProductHCID 90032105HCID 9003210519.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

0.094 g (0.352 mmol) of 2-(chloromethyl)-3-(phenylethynyl)imidazo[1,2-a]pyridine were dissolved in 2 ml of dimethylformamide with magnetic stirring, 121 mg (0.529 mmol) of N-(3-hydroxyphenyl)methanesulfonamide and 0.172 g (0.529 mmol) of cesium carbonate were added. The mixture was stirred at 60° C. for 3 h before being poured onto 15 ml of a saturated NaCl aqueous solution. The aqueous phase was extracted with 2×20 ml of ethyl acetate. The combined organic phases were dried on Na2SO4 which was then removed by filtration. The obtained filtrate was concentrated in vacuo. The crude residue was purified by preparative HPLC and 0.028 g (yield=18%) of N-(3-((3-(phenylethynyl)imidazo[1,2-a]pyridin-2-yl)-methoxy)phenyl)methane sulfonamide were obtained as a white solid. LC-MS: m/z=418 (MH+); UV purity at 254 nm=95%. 1H NMR (300 MHz, DMSO) δ 9.53 (s, 1H), 8.55 (d, J=6.8 Hz, 1H), 7.76-7.57 (m, 3H), 7.54-7.33 (m, 4H), 7.17-7.02 (m, 2H), 6.89 (dd, J=8.0, 1.1 Hz, 1H), 6.79 (t, J=2.1 Hz, 1H), 6.69-6.54 (m, 1H), 5.07 (s, 2H), 3.14 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09381191B2
Source datasetuspto-grants-2016_07
ORD IDord-3f0da7abbd0942c792248ff0e7fc9fd2
Source noteuspto-grants-2016_07