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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458898Generated: October 25, 2026

Water → 5-(2,5-Dimethoxybenzylamino)-6-diphenylmethyl-1-azabicyclo-[2.2.2]octane-3-carboxamide

https://huagongshe.com/reaction/1458898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,5-DimethoxybenzenemethanamineHCID 18652—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN,N-Dimethyl-6-diphenylmethyl-5-oxo-1-azabicyclo[2.2.2]-octane-3-carboxamideHCID 22097572—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
Product5-(2,5-Dimethoxybenzylamino)-6-diphenylmethyl-1-azabicyclo-[2.2.2]octane-3-carboxamideHCID 1970153219%

Reaction Steps

A mixture of 48 (1.2 g, 3 mmol), 2,5-dimethoxybenzyl amine (0.6 g, 3.3 mmol) camphor sulfonic acid (45 mg) in toluene (15 ml) was heated at reflux with removal of water for 3 hours and then the solvent was removed. The residue was dissolved in small amount of THF (3 ml) and this solution was added to a solution of sodium triacetoxyborohydride (1.7 g, 8 mmol) in acetic acid (40 ml) at room temperature. The mixture was stirred at room temperature for 3 hours and the solvent was removed. Water was added and the mixture was neutralized with NaHCO3 and extracted with EtOAc three times. The combined extracts were dried over Na2SO4 and concentrated. Recrystallization from MeOH/acetone to give by-product. The mother liquor was concentrated and the residue was purified by recrystallization from MeOH/EtOAc to give 50 (0.27 g, 0.56 mmol, 19%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852038
Source datasetuspto-grants-1998_12
ORD IDord-562fa990bcdc4a8e8c98106cdd4c336c
Source noteuspto-grants-1998_12