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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703707Generated: October 25, 2026

Methanol → 1-Methyl-3-{N-[[beta-[3,4-bis(isobutyryloxy)phenyl]ethyl]]carbamoyl}-1,4-dihydropyridine

https://huagongshe.com/reaction/703707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium DithioniteHCID 24489—
ReactantSodium BicarbonateHCID 516892—
Reactant1-methyl-3-{N-[[beta-[3,4-bis(isobutyryloxy)phenyl]ethyl]]carbamoyl}-pyridinium trifluoroacetateHCID 14050431—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-Methyl-3-{N-[[beta-[3,4-bis(isobutyryloxy)phenyl]ethyl]]carbamoyl}-1,4-dihydropyridineHCID 14050430—

Reaction Steps

A solution of 0.55 g (1 mmol) of 1-methyl-3-{N-[[β-[3,4-bis(isobutyryloxy)phenyl]ethyl]]}carbamoylpyridinium trifluoroacetate in 50 mL of deaerated water containing 10 mL of methanol was extracted three times with 30 mL portions of ether. To the resultant aqueous solution were added NaHCO3 (0.25 g, 3 mmol) and 50 mL of ethyl ether and the mixture was kept under nitrogen. To this ice-cold mixture was added sodium dithionite (0.52 g, 3 mmol) and the mixture was stirred vigorously for 30 minutes. The ether layer was separated and the aqueous layer was extracted twice with ether. The combined ether extracts were washed with water and dried over sodium sulfate. Ether was removed under vacuum, leaving an oily product. NMR analysis confirmed that the product had the structural formula: ##STR69##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983586
Source datasetuspto-grants-1991_01
ORD IDord-9f161248d96d4181bf8ec609071d9339
Source noteuspto-grants-1991_01