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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350910Generated: November 3, 2026

Sodium borohydride → HCID 23599483, compound

https://huagongshe.com/reaction/1350910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23599482HCID 23599482—
SolventMethanolHCID 887—
ProductHCID 23599483HCID 2359948362.1%

Reaction Steps

To the solution of (R)-N-(1-azabicyclo[2.2.2]oct-3-yl)(5-(3-formylphenyl)thiophene-2-carboxamide) (875 mg) in methanol (15 mL), sodium borohydride (97.2 mg) was added. The mixture was then stirred at room temperature for 4 h. The residue was partitioned between water and chloroform. The extracts were dried over magnesium sulfate, filtered, and evaporated, and the residue was then purified by flash chromatography using 5–20% 3.5M methanolic ammonia/chloroform mixtures as the eluent to give the title compound (547 mg); MS (ES+) 343 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214688B2
Source datasetuspto-grants-2007_05
ORD IDord-822056e8e1c04ae687f52d7738130b2a
Source noteuspto-grants-2007_05