돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 416887생성일: 2026년 10월 26일

Diisopropylethylamine → tert-Butyl 4-((2-isopropyloxazol-4-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/416887

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물4-(Chloromethyl)-2-(propan-2-yl)-1,3-oxazoleHCID 2763291—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물tert-Butyl 4-((2-isopropyloxazol-4-yl)methyl)piperazine-1-carboxylateHCID 4686702099%

반응 조건

온도35 °C

반응 단계

4-(Chloromethyl)-2-isopropyloxazole (0.920 g, 5.75 mmol, 1 eq) was suspended in DCM (9 mL). DIPEA (2.5 mL, 14.4 mmol, 2.5 eq) was added dropwise, followed by N-Boc-piperazine (2.350 g, 12.6 mmol, 2.2 eq). The reaction mixture was stirred at 35° C. for 17 h, then diluted with EtOAc, washed with H2O, and brine. The organic layer was separated, dried (MgSO4) and the solvent removed in vacuo. The crude product was purified by column chromatography on a Biotage SP1 system (DCM/EtOAc; v/v 1:1) to give the title compound (1.760 g, 99%); 1H-NMR (500 MHz, CDCl3): δ 1.33 (d, J=5.5 Hz, 6H, iPr—CH3), 1.45 (s, 9H, C(CH3)3), 2.45 (br t, J=4.8 Hz, 4H, piperazine N(CH2)2), 3.07 (m, 1H, iPr—CH), 3.41-3.50 (m, 6H, piperazine N(CH2)2 and NCH2), 7.41 (s, 1H, oxazole 5-H); LC (Method B)-MS (ESI, m/z): Rt=2.51 min—310 [(M+H)+, 100%].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088761B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-f5b8115fff534e14913fab0c94b18b51
출처 메모uspto-grants-2012_01