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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361463Generated: October 30, 2026

Ethanol → HCID 21186252, compound

https://huagongshe.com/reaction/361463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantIsobutyl (2-chloropyridin-3-yl)sulfonyl(3-methoxy-5-methylpyrazin-2-yl)carbamateHCID 11015197—
ReactantHCID 21186218HCID 21186218—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 21186252HCID 2118625239%

Reaction Conditions

Temperature80 °C

Reaction Steps

Tetrakis(triphenylphosphine)palladium (0) (500 mg) was added to a deoxygenated solution of sodium carbonate (3.74 g), 4-(2-carboxypropyl)phenyl boronic acid (3.67 g) and 2-chloro-N-(isobutoxycarbonyl)-N-(3-methoxy-5-methyl-pyrazin-2-yl)pyridine-3-sulphonamide (6.1 g) in a mixture of water (30 ml), ethanol (75 ml) and toluene (75 ml). The mixture was stirred and heated under argon at 80° C. for 17 hours and then allowed to cool to ambient temperature. Ice water (5 g) was added and the reaction extracted with ethyl acetate (75 ml). The combined organic layers were extracted with saturated aqueous sodium carbonate solution (2×15 ml) and combined aqueous extracts were acidified to pH 2 with 2M hydrochloric-acid and extracted with ethyl acetate (3×100 ml). The combined organic extracts were dried (MgSO4) and evaporated to low volume affording crystalline material which was filtered and washed with diethyl ether to give N-(isobutoxycarbonyl)-2-(4-(2-carboxypropyl)phenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (3.11 g); NMR 1H (d6 -DMSO): 0.61 (d, 6 H), 1.09 (d, 3 H), 1.50-1.73 (m, 1 H), 2.55 (partly obscured by DMSO, 3 H), 2.6-2.77 (m, 2 H), 2.72-3.09 (m, 1 H), 2.83 (d, 2 H), 3.96 (s, 3 H), 7.25 (d, 2 H), 7.43 (d, 2 H), 7.78 (dd, 1 H), 8.15 (s, 1 H), 8.83-8.96 (m, 2 H), 12.14 (br s, 1 H); mass spectrum (-ve ESP) 541.1 (M-H )-.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866568
Source datasetuspto-grants-1999_02
ORD IDord-2d6153a3662d44299c6fb0fd6a8d2327
Source noteuspto-grants-1999_02