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HRID 84732作成日:2026年10月25日

N-methyl-2-pyrrolidone → 3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide

https://huagongshe.com/reaction/84732

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物3-Iodo-5-nitrobenzoic acidHCID 80580—
反応物MethoxyisopropylamineHCID 123458—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamideHCID 5785131927.9%

反応手順

EDCI (7.07 g, 36.9 mmol) was added in one portion to a stirred solution of 3-Iodo-5-nitro-benzoic acid (2.31 g, 24.6 mmol), HOBt (4.985 g, 36.9 mmol), 2-Amino-1-methoxypropane (2.73 ml, 24.6 mmol) and NMP (4.06 ml 36.9 mmol) in CH2Cl2 (120 ml) and DMF (10 ml) at 0° C. The reaction was allowed to warm to room temperature and was stirred over night. The reaction mixture was then washed with 2N NaOH, water, brine, and dried over Na2SO4. Solvent was removed in vacuo to give 2.50 g of 3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide as a yellow solid, MS (M+H)=365. This material was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846945B2
出典データセットuspto-grants-2014_09
ORD IDord-0d9589c7e058451894f1ce443e0d8999
出典メモuspto-grants-2014_09