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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726332Generated: November 1, 2026

Diisopropylethylamine → HCID 9836523, compound

https://huagongshe.com/reaction/1726332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromothiophene-2-carboxylic acidHCID 349115—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(R)-(+)-3-Aminoquinuclidine DihydrochlorideHCID 12494972—
SolventDimethylformamideHCID 6228—
ProductHCID 9836523HCID 983652392.7%

Reaction Steps

A mixture of (R)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride (4 g), 5-bromothiophene-2-carboxylic acid (4.25 g), 1-hydroxybenzotriazole hydrate (2.77 g), O-benzotriazol-1-yl-N,N,N′-tetramethyluronium tetrafluoroborate (6.6 g), and N,N-diisopropylethylamine (14 mL), in N,N-dimethylformamide (100 mL) was stirred at room temperature overnight. The solution was evaporated, and the residue was partitioned between aqueous sodium hydroxide and chloroform. The chloroform layer was dried over magnesium sulfate, filtered, and evaporated. The residue was purified by flash chromatography on silica gel and eluted with 5%-20% 3.5N methanolic ammonia/chloroform mixtures. Evaporation of solvent gave yellow solid (5.87 g); MS (ES+) 315, 317 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491734B2
Source datasetuspto-grants-2009_02
ORD IDord-a11c68db21234bbd8e69ee05b855610e
Source noteuspto-grants-2009_02