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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704081Generated: October 27, 2026

Sodium Hydroxide → HCID 15713338, compound

https://huagongshe.com/reaction/704081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
ReactantCyano-borohydrideHCID 498716—
ReactantN-(4-methylpyridazino[4,5-b]indolizin-1-yl)-1,2-ethanediamineHCID 20075512—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
ProductHCID 15713338HCID 15713338—

Reaction Steps

To a solution of 3-quinuclidinone hydrochloride (600 mg, 3.7 mmol) in methanol (15 mL) was added a solution of N-(4-methylpyridazino[4,5-b]indolizin-1-yl)-1,2-ethanediamine (900 mg, 3.7 mmol) in methanol (11 mL) over a one minute period at room temperature. After stirring for 5 to 10 minutes, a solution of zinc modified cyanoborohydride (8.7 mL of 0.50M cyanoborohydride in methanol, 4.4 mmol) was added [Kim, et al., J. Org. Chem. 50, 1927 (1985)]. A yellow precipitate formed. After stirring for 4 days at room temperature, 50% sodium hydroxide (1 mL) was added and the solvent was evaporated. The residue was mixed with 4:1 chloroform:methanol (at 20 mL) and filtered through a plug of basic alumina. The filtrate was evaporated and the residue was purified by flash chromatography (alumina, 4:1 chloroform:methanol to 100% methanol) to give the title compound as the free base which was converted to the fumaric acid salt (fumaric acid/ethanol), mp 205°-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985560
Source datasetuspto-grants-1991_01
ORD IDord-d588fe74538b4ef1a911401496c06855
Source noteuspto-grants-1991_01