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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563931Generated: October 25, 2026

Sulfuric Acid → Sulfate Ion

https://huagongshe.com/reaction/563931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPalosuranHCID 10173280—
SolventMethanolHCID 887—
ProductSulfate IonHCID 1117—
ProductPalosuranHCID 10173280—

Reaction Conditions

Temperature-2 °C

Reaction Steps

To a suspension of 1-[2-(4-benzyl-4-hydroxy-piperidin-1-yl)-ethyl]-3-(2-methyl-quinolin-4-yl)-urea (21.36 kg) in CH3OH (178 L) is added aqueous H2SO4 (6 L, 9.91%) during 10 min. The clear solution is filtered and further aqueous H2SO4 (33.8 L, 1.07 M) is added during 45 min. The solution is cooled to −2° C. during 1.5 h and stirred at −5 to −9° C. for 1 h. The formed precipitate is filtered, washed with cooled CH3OH (−5° C., 54 L) and dried under a stream of nitrogen provide 1-[2-(4-benzyl-4-hydroxy-piperidin-1-yl)-ethyl]-3-(2-methyl-quinolin-4-yl)-urea of formula I sulfate as a non-defined hydrate. A slurry of the so obtained salt in H2O (16.2% w/w) is stirred for 3 days at 25° C. Filtration and drying at 30° C. under a wet stream of nitrogen (50% RH) provides the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067601B2
Source datasetuspto-grants-2011_11
ORD IDord-9e26d5cc05f94d419fbf35cc3efed69f
Source noteuspto-grants-2011_11