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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107649Generated: October 31, 2026

Methanesulfonic Acid → HCID 10412674, compound

https://huagongshe.com/reaction/2107649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15257493HCID 15257493—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 10412674HCID 1041267479.3%

Reaction Steps

To a stirred solution of 1-[2-[5-[3,5-dimethoxy-4-{(2-methoxyethoxy)methoxy}phenyl]-(2E,4E)-2,4-pentadienoylamino]ethyl]-4-(3-indolyl)piperidine (10.0 g) in methanol (100 ml) was added slowly methanesulfonic acid (2.3 ml) at ambient temperature. After stirring for 2 hours, the reaction mixture was adjusted to pH 7.2 with aqueous 2N sodium hydroxide solution, and poured into a solution of 4.5 g of sodium bicarbonate in 500 ml of water. After stirring for 30 minutes, the resulting precipitate was collected by filtration and washed with 100 ml of water. The residue was subjected to column chromatography on silica gel and eluted with a mixture of chloroform and methanol. The fractions containing the object compound were combined and concentrated under reduced pressure. The residue was recrystallized from ethanol to give 1-[2-{5-(4-hydroxy-3,5-dimethoxyphenyl)-(2E,4E)-2,4-pentadienoylamino}ethyl]-4-(3-indolyl)piperidine (6.69 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935432
Source datasetuspto-grants-1990_06
ORD IDord-40ecf01fd9d04b329191e6a729d3a415
Source noteuspto-grants-1990_06