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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369903Generated: October 30, 2026

Sodium hydride → HCID 70896185, compound

https://huagongshe.com/reaction/2369903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(3S)-1-azabicyclo[2.2.2]octan-3-amine dihydrochlorideHCID 12494973—
ReactantHCID 86672705HCID 86672705—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 70896185HCID 7089618587%

Reaction Steps

To a stirred solution of (S)-(−)-3-aminoquinuclidine dihydrochloride (0.2 g, 0.8 mmol) in methylene chloride (2 mL) was added sodium hydride (0.1 g, 1.6 mmol) and the mixture was stirred for 2 h. A solution of methyl 1-(2-oxoethyl)-1H-benzo[d]imidazole-7-carboxylate (0.2 g, 0.7 mmol) from Step E above in methylene chloride (3 mL) was added followed by acetic acid (0.7 mL) and the mixture was stirred at room temperature for 4 h. Sodium triacetoxyborohydride (0.4 g, 2.1 mmol) was then added in portions and the reaction was stirred at room temperature overnight. The crude reaction was quenched with methanol, concentrated under reduced pressure, and purified by preparative thin layer chromatography (90:9:1 methylene chloride/methanol/ammonium hydroxide) to afford (S)-methyl 1-(2-(quinuclidin-3-ylamino)ethyl)-1H-benzo[d]imidazole-7-carboxylate (0.2 g, quantitative yield): MS (ESI+) m/z 329 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710046B2
Source datasetuspto-grants-2014_04
ORD IDord-bd95cafdb5eb495487a1e979eabe4815
Source noteuspto-grants-2014_04