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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846804Generated: October 30, 2026

Sulfuric Acid → HCID 86744270, compound

https://huagongshe.com/reaction/846804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 15096820HCID 15096820—
ProductHCID 86744270HCID 86744270—

Reaction Steps

To 65 parts of a sulfuric acid solution 96% were added portionwise (slowly) 3.6 parts of cis-4-amino-5-cyano-N-[1-[(4-fluorophenyl)methyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide while cooling in an ice-bath. The reaction mixture was allowed to reach room temperature and stirring was continued for 7 hours at room temperature. The reaction mixture was poured onto crushed ice and the whole was alkalized with ammonium hydroxide. The product was extracted with trichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The most pure fractions were collected and the eluent was evaporated. The residue was further purified by HPLC using a mixture of methylbenzene and ethanol (90:10 by volume) as eluent. The pure fraction was collected and the eluent was evaporated. The residue was boiled in acetonitrile. The product was filtered off and dried, yielding 2.67 parts of cis-4-amino-N1 -[1-[(4-fluorophenyl)methyl]-3-methoxy-4-piperidinyl] -6-methoxy-1,3-benzenedicarboxamide; mp. 243.7° C. (compound 234).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137896
Source datasetuspto-grants-1992_08
ORD IDord-3882a2987bac4e9bb59c9a8917ed2415
Source noteuspto-grants-1992_08