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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 534783생성일: 2026년 10월 26일

Triethylamine → 1,1-Dimethylethyl (2S)-4-[(4-amino-2-chlorophenyl)methyl]-2-methyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/534783

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,1-Dimethylethyl (2S)-4-[(2-chloro-4-nitrophenyl)methyl]-2-methyl-1-piperazinecarboxylateHCID 59262128—
촉매PlatinumHCID 23939—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물1,1-Dimethylethyl (2S)-4-[(4-amino-2-chlorophenyl)methyl]-2-methyl-1-piperazinecarboxylateHCID 5926213268.4%

반응 단계

A mixture of 1,1-dimethylethyl (2S)-4-[(2-chloro-4-nitrophenyl)methyl]-2-methyl-1-piperazinecarboxylate (D103) (0.199 g, 0.538 mmol), triethylamine (0.75 mL, 5.38 mmol) and 5% Pt/C catalyst (0.134 g) in MeOH (5 mL) was hydrogenated at room temperature and atmospheric pressure for 3 h. The catalyst was removed by filtration and the filtrate was concentrated to give a colourless oil which was dissolved in DCM. The DCM solution was washed with water (×2) and brine, then dried and concentrated to give the crude product. Purification by column chromatography eluting with 10-40% EtOAc/pentane gave the title compound as a colourless oil (0.125 g). δH (CDCl3, 400 MHz) 7.19 (1H, d), 6.69 (1H, d), 6.54 (1H, dd), 4.18 (1H, br.s), 3.79 (1H, d), 3.70 (2H, br.s), 3.45 (2H, m), 3.07 (1H, td), 2.74 (1H, m), 2.60 (1H, m), 2.19 (1H, dd), 2.03 (1H, m), 1.45 (9H, s), 1.22 (3H, d). MS (ES): MH+ 340/342.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853218B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-39685093be8548b68e28fc124bdc676f
출처 메모uspto-grants-2014_10