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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388314생성일: 2026년 10월 26일

Diisopropylethylamine → tert-butyl 4-(N-(4-chlorobenzyl)-N-(2-(diethylamino)ethyl)carbamoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/388314

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N-[(4-chlorophenyl)methyl]-N',N'-diethylethane-1,2-diamineHCID 296048—
반응물Tert-butyl 4-(chlorocarbonyl)piperazine-1-carboxylateHCID 11334154—
용매DichloromethaneHCID 6344—
생성물tert-butyl 4-(N-(4-chlorobenzyl)-N-(2-(diethylamino)ethyl)carbamoyl)piperazine-1-carboxylateHCID 6713506745%

반응 단계

tert-Butyl 4-chlorocarbonyl-piperazine-1-carboxylate (245 mg, 0.99 mmol) was added to a solution of N1-(4-chlorobenzyl)-N2,N2-diethylethane-1,2-diamine (235 mg, 0.98 mmol) and N,N-diisopropylethylamine (0.54 mL, 2.94 mmol) in DCM (2 mL). The reaction mixture was allowed to stir at room temperature for 1 hour. The mixture was quenched with saturated NH4Cl (2 mL) and extracted with DCM (2×5 mL). The combined organics were dried (Na2SO4), filtered and concentrated. The crude product was purified by silica gel chromatography to give tert-butyl 4-(N-(4-chlorobenzyl)-N-(2-(diethylamino)ethyl)carbamoyl)piperazine-1-carboxylate (200 mg, 45%). 1H NMR (CDCl3, 400 MHz) 7.32 (d, J=8.4 Hz, 2 H), 7.19 (d, J=8.4 Hz, 2 H), 4.42 (s, 2 H), 3.45-3.40 (m, 4 H), 3.25-3.20 (m, 4 H), 3.18 (t, J=6.8 Hz, 2 Hz), 2.56 (t, J=6.8 Hz, 2 H), 2.49 (q, J=7.2 Hz, 4 H), 1.46 (s, 9 H), 0.99 (t, J=7.2 Hz, 6 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08377937B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-de5971f03d954093b980948740065b31
출처 메모uspto-grants-2013_02