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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165046Generated: October 31, 2026

Hydrochloric Acid → HCID 14855009, compound

https://huagongshe.com/reaction/1165046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant2-ChloropyrimidineHCID 74404—
ReactantHCID 14854956HCID 14854956—
CatalystDimethylacetamideHCID 31374—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14855009HCID 1485500924.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4.6 parts of cis-4-amino-N-[1-(4-aminobutyl)-3-methoxy-4-piperidinyl]-5-chloro-2-methoxybenzamide, 1.4 parts of 2-chloropyrimidine and a few drops of N,N-dimethylacetamide was stirred overnight at 80° C. The reaction mixture was taken up in a mixture of dichloromethane, water and hydrochloric acid. The separated aqueous layer was treated with sodium carbonate and 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, methanol and methanol, saturated with ammonia, (96:3:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 1.34 parts (24.1%) of cis-4-amino-5-chloro-2-methoxy-N-[3-methoxy-1-[4-(2-pyrimidinylamino)butyl]-4-piperidinyl]benzamide; mp. 114.8° C. (compound 29).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906643
Source datasetuspto-grants-1990_03
ORD IDord-d6b346ce10914715ba20b7fe964ba295
Source noteuspto-grants-1990_03