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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165044Generated: October 27, 2026

Potassium Iodide → cis-4-amino-5-chloro-2-methoxy-N-[3-methoxy-1-[2-[(3-methyl-2-pyrazinyl)amino]ethyl]-4-piperidinyl]benzamide

https://huagongshe.com/reaction/1165044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Bromo-3-methylpyrazineHCID 12457513—
Reactantcis-4-amino-N-[1-(2-aminoethyl)-3-methoxy-4-piperidinyl]-5-chloro-2-methoxybenzamideHCID 14854954—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productcis-4-amino-5-chloro-2-methoxy-N-[3-methoxy-1-[2-[(3-methyl-2-pyrazinyl)amino]ethyl]-4-piperidinyl]benzamideHCID 1485502136%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 8.56 parts of 2-bromo-3-methylpyrazine and 0.1 parts of potassium iodide was pulverized and 2 parts of cis-4-amino-N-[1-(2-aminoethyl)-3-methoxy-4-piperidinyl]-5-chloro-2-methoxybenzamide were added. The whole was stirred for 3 hours at 120° C. The reaction mixture was taken up in dichloromethane and water and made alkaline with ammonium hydroxide. The organic layer was separated, washed with water, 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 first fractions was collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 1.95 parts (36%) of cis-4-amino-5-chloro-2-methoxy-N-[3-methoxy-1-[2-[(3-methyl-2-pyrazinyl)amino]ethyl]-4-piperidinyl]benzamide; mp. 169.5° C. (compound 27).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906643
Source datasetuspto-grants-1990_03
ORD IDord-2aa1dc1a14994f909e4754acb813cc6a
Source noteuspto-grants-1990_03