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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281181Generated: October 27, 2026

1,2-Dichloroethane → 4-Amino-N-(1-azabicyclo[2.2.2]oct-3-yl)-3-iodobenzamide

https://huagongshe.com/reaction/2281181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-Amino-3-iodobenzoic AcidHCID 16461—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantQuinuclidine, 3-amino-, dihydrochlorideHCID 197853—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Amino-N-(1-azabicyclo[2.2.2]oct-3-yl)-3-iodobenzamideHCID 5893294390.2%

Reaction Steps

A solution of 2.04 g (10.3 mmol) of 3-aminoquinuclidine dihydrochloride, 2.70 g (10.3 mmol) of 4-amino-3-iodobenzoic acid, 1.39 g (10.3 mmol) of HOBt, 2.16 g (11.3 mmol) of EDC and 6.63 g (51.3 mmol) of N,N-diisopropylethylamine in 150 ml of DMF was stirred at room temperature for 16 h. 300 ml of water were added, and the aqueous phase was extracted three times with 300 ml of ethyl acetate each time. The combined organic phases were dried over sodium sulfate and the solvent was distilled off in vacuo. The residue was purified on a flash column (mobile phase: dichloromethane/methanol/triethylamine 90:10:0.2). 3.45 g (87%) of the desired title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139579B2
Source datasetuspto-grants-2015_09
ORD IDord-bd76d74d0f2c406d8dcb04710c28358c
Source noteuspto-grants-2015_09