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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891440Generated: October 30, 2026

5-Bromothiophene-3-carboxylic acid → HCID 23599495, compound

https://huagongshe.com/reaction/891440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromothiophene-3-carboxylic acidHCID 12039978—
Reactant(R)-(+)-3-Aminoquinuclidine DihydrochlorideHCID 12494972—
ProductHCID 23599495HCID 23599495—

Reaction Steps

Prepared by a method analogous to that described for the preparation of Intermediate 1 from (R)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride and 5-bromothiophene-3-carboxylic acid. The compound was purified by reverse phase HPLC on a Waters Bondapak® C18 column using a gradient of acetonitrile and 0.1% aqueous trifluoroacetic acid as the eluent. The product-containing fractions were evaporated, the residues dissolved in methanol, excess hydrogen chloride solution (4M in 1,4-dioxane) was added and the solution was evaporated. After drying under vacuum, the hydrochloride salt of the title compound was obtained as a colourless solid; MS (ES+) 315, 317 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001914B2
Source datasetuspto-grants-2006_02
ORD IDord-d56ed7e9f2fd462791ab56c020dcf2ad
Source noteuspto-grants-2006_02