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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345587Generated: October 25, 2026

Potassium Iodide → Alimix

https://huagongshe.com/reaction/345587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-(3-Chloropropoxy)-4-fluorobenzeneHCID 74391—
Reactant4-Amino-5-chloro-2-methoxy-N-[(3R,4S)-3-methoxypiperidin-4-YL]benzamideHCID 9861621—
SolventTriethylamineHCID 8471—
ProductAlimixHCID 1367777842.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4.7 parts of 1-(3-chloropropoxy)-4-fluorobenzene, 3.015 parts of cis-4-amino-5-chloro-2-methoxy-N-(3-methoxy-4-piperidinyl)benzamide, 0.1 parts of potassium iodide, 3 parts of N,N-diethylethanamine and 45 parts of N,N-dimethylformiade was stirred and heated for 18 hours at 60° C. The reaction mixture was poured onto water. The precipitated product was filtered off and dissolved in trichloromethane. The solution was washed with water. The organic phase was separated, 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 pure fractions were collected and the eluent was evaporated. The oily residue was crystallized from 2-propanol. The product was filtered off and dried, yielding 3.11 parts (42.8%) of cis-4-amino-5-chloro-N-[1-[3-(4-fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide monohydrate; mp. 109.8° C. (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057525
Source datasetuspto-grants-1991_10
ORD IDord-a36337ea83e14c01b1b64194d4dd7c8a
Source noteuspto-grants-1991_10