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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107471Generated: November 1, 2026

Ammonium Chloride → HCID 21186248, compound

https://huagongshe.com/reaction/1107471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 21186304HCID 21186304—
SolventMethanolHCID 887—
ProductHCID 21186248HCID 2118624861.4%

Reaction Steps

Sodium methoxide (0.115 g) was added to a solution of 2-[4-(N,N-dimethylamino)phenyl]-N-(isobutoxycarbonyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (0.212 g) in methanol (10 ml) and the mixture was stirred and heated under reflux for 90 minutes. The reaction mixture was cooled, poured into saturated aqueous ammonium chloride solution (30 ml) and extracted with ethyl acetate (3×30 ml). The organic extracts were combined and dried (MgSO4). Volatile material was removed by evaporation and the residue was triturated with ether to give 2-[4-(N,N-dimethylamino)phenyl]-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (104 mg) as a solid, m.p. 183-184.5° C.; 1H NMR (d6 -DMSO): 2.2 (s, 3H), 2.95 (s, 6H), 3.8 (s, 3H), 6.7 (br s, 2H), 7.3-7.5 (m, 4H), 8.37 (dd, 1H), 8.7 (dd, 1H), 10.1 (br s, 1H); mass spectrum (+ve FAB, DMSO/methanol/NBA): 400 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060475
Source datasetuspto-grants-2000_05
ORD IDord-a722b1321b0c4b8a8e7d3a41ebb635fe
Source noteuspto-grants-2000_05