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HRID 854099作成日:2026年10月25日

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

https://huagongshe.com/reaction/854099

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物4-Amino-3-iodobenzoic AcidHCID 16461—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物Quinuclidine, 3-amino-, dihydrochlorideHCID 197853—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-Amino-N-(1-azabicyclo[2.2.2]oct-3-yl)-3-iodobenzamideHCID 58932943—

反応手順

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 obtined.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07256288B2
出典データセットuspto-grants-2007_08
ORD IDord-cf406bb05eee4892a96ab2106020c65f
出典メモuspto-grants-2007_08