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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107648Generated: October 30, 2026

Methanesulfonic Acid → HCID 10530187, compound

https://huagongshe.com/reaction/2107648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23046195HCID 23046195—
SolventMethanolHCID 887—
ProductHCID 10530187HCID 1053018765.3%

Reaction Steps

To a solution of 1-[2-[5-[3,5-di-tert-butyl-4-{(2-methoxyethoxy)methoxy}phenyl]-(2E,4E)-2,4-pentadienoylamino]ethyl]-4-(3-indolyl)piperidine (0.5 g) in methanol (5 ml) was added dropwise methanesulfonic acid (0.26 ml) at 18°-25° C. After 2 hours the reaction mixture was adjusted to pH 7.5 with 2N-sodium hydroxide and then poured into saturated sodium bicarbonate solution (50 ml). The resulting precipitate was collected and washed with water. The precipitate was subjected to column chromatography on silica gel and eluted with a mixture of chloroform and methanol (20:1, V/V). The fractions containing the object compound were combined and concentrated under reduced pressure. The residue was recrystallized from 1,4-dioxane, to give white crystals of 1-[2-{5-(3,5-di-tert-butyl-4-hydroxyphenyl)-(2E,4E)-2,4-pentadienoylamino}ethyl]-4-(3-indolyl)piperidine (0.28 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935432
Source datasetuspto-grants-1990_06
ORD IDord-9b45e44039284f9086285835e29a2af3
Source noteuspto-grants-1990_06