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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552131생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/552131

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Bromodifluoroacetyl chlorideHCID 520892—
반응물4-(2-Iodophenylamino)piperidine-1-carboxylic acid tert-butyl esterHCID 43652179—
용매DichloromethaneHCID 6344—
생성물4-[(2-Bromo-2,2-difluoroacetyl)-(2-iodophenyl)amino]piperidine-1-carboxylic acid tert-butyl esterHCID 6717168283.6%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951805B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-97851995b6b74204aa007a95ac674fa5
출처 메모uspto-grants-2011_05