戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 552131作成日:2026年10月25日

Triethylamine → 4-[(2-Bromo-2,2-difluoroacetyl)-(2-iodophenyl)amino]piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/552131

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Bromodifluoroacetyl chlorideHCID 520892—
反応物4-(2-Iodophenylamino)piperidine-1-carboxylic acid tert-butyl esterHCID 43652179—
溶媒DichloromethaneHCID 6344—
生成物4-[(2-Bromo-2,2-difluoroacetyl)-(2-iodophenyl)amino]piperidine-1-carboxylic acid tert-butyl esterHCID 6717168283.6%

反応手順

Bromodifluoroacetyl chloride (0.800 g, 4.1 mmol) was added dropwise to a cooled (0° C.) solution of 4-(2-Iodophenylamino)piperidine-1-carboxylic acid tert-butyl ester (1.500 g, 3.7 mmol) and triethylamine (1.0 mL, 7.1 mmol) in dichloromethane (20 mL). The cooling bath was removed 30 minutes after the addition of all reagents. The reaction mixture was stirred at ambient temperature for 1 hour, then diluted with ethyl acetate, washed with water and brine, dried over anhydrous Na2SO4 and concentrated. Purification of the residue by flash chromatography to afford 4-[(2-bromo-2,2-difluoroacetyl)-(2-iodophenyl)amino]piperidine-1-carboxylic acid tert-butyl ester (1.730 g, 83%). 1H NMR (300 MHz, CDCl3) δ 7.88 (dd, J=1.2 and 7.8 Hz, 1H), 7.41-7.06 (m, 3H), 4.45-4.37 (m, 1H), 4.17-4.03 (m, 2H), 2.81-2.64 (m, 2H), 2.18-2.12 (m, 1H), 1.89-1.84 (m, 1H), 1.59-1.52 (m, 1H), 1.40 (s, 9H), 1.25-0.98 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951805B2
出典データセットuspto-grants-2011_05
ORD IDord-97851995b6b74204aa007a95ac674fa5
出典メモuspto-grants-2011_05