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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166369Generated: November 3, 2026

Water → HCID 178491241, compound

https://huagongshe.com/reaction/1166369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(Methylsulfonyl)aniline hydrochlorideHCID 2735180—
Reactant2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 178491241HCID 178491241—

Reaction Steps

To a suspension of 4-(methylsulfonyl)aniline hydrochloride (1.8 g, 8.7 mmol) in toluene (50 ml) at 0° C., trimethylaluminum (2M solution in toluene, 5.2 ml, 10.4 mmol) was added over 10 minutes. The reaction mixture was warmed to room temperature and stirred for 2 hours. A solution of 6-methoxy-3-cyanopyridine (1.75 g, 13 mmol) in toluene (100 ml) was added over 10 minutes and the mixture was heated to 85-90° C. After 24 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride and methanol and later with methanol. The combined filtrates were concentrated and the resulting yellowish solid was stirred with ethyl acetate (1000 ml) and filtered. The white solid (2 g, 75%) was used in the next reaction without further purification. Anal. Calc'd. for C14H16N3SClO3.0.5 H2O: C, 47.93, H, 4.88, N, 11.98. Found: C, 48.01, H, 4.82, N, 11.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613789B2
Source datasetuspto-grants-2003_09
ORD IDord-e78d9b05a98d41aba2592f84ec27f660
Source noteuspto-grants-2003_09