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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110393Generated: November 3, 2026

Potassium Iodide → HCID 86744369, compound

https://huagongshe.com/reaction/1110393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantTriethylamineHCID 8471—
Reactant4-Amino-5-chloro-2-methoxy-N-[(3R,4S)-3-methoxypiperidin-4-YL]benzamideHCID 9861621—
ReactantHCID 16780864HCID 16780864—
SolventDimethylformamideHCID 6228—
ProductHCID 86744369HCID 86744369—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2.54 parts of 4-chloro-N-methyl-N-phenylbutanamide, 3.14 parts of cis-4-amino-5-chloro-2-methoxy-N-(3-methoxy-4-piperidinyl)benzamide, 2.45 parts of N,N-diethylethanamine, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylformamide was stirred for 20 hours at 80° C. The reaction mixture was evaporated. The residue was taken up in water and sodium carbonate. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile and a small amount of water. The product was filtered off and dried, yielding 2.05 parts (40.4%) of cis-4-[4-amino-5-chloro-2-methoxybenzoyl)amino]3-methoxy-N-methyl-N-phenyl-1-piperidinebutanamide monohydrate; mp. 97.4° C. (compound 23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04975439
Source datasetuspto-grants-1990_12
ORD IDord-eec52c55a0a74e8e8a3083c6f8eea4ff
Source noteuspto-grants-1990_12