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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| 반응물 | 4-(Chloromethyl)-2-(propan-2-yl)-1,3-oxazole | HCID 2763291 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | tert-Butyl 4-((2-isopropyloxazol-4-yl)methyl)piperazine-1-carboxylate | HCID 46867020 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08088761B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-f5b8115fff534e14913fab0c94b18b51 |
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| 출처 메모 | uspto-grants-2012_01 |
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