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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1794125생성일: 2026년 10월 25일

3-Fluorobenzyl chloride → 2,6-Difluoro-4-(3-fluorobenzyl)oxybenzyl cis-2,6-dimethylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1794125

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluorobenzyl chlorideHCID 9974—
반응물rac-tert-butyl (3R,5S)-4-(carboxy)-3,5-dimethylpiperazine-1-carboxylateHCID 22219933—
반응물3,5-Difluoro-4-(hydroxymethyl)phenolHCID 22219975—
생성물2,6-Difluoro-4-(3-fluorobenzyl)oxybenzyl cis-2,6-dimethylpiperazine-1-carboxylateHCID 69142679—

반응 단계

2,6-Difluoro-4-(3-fluorobenzyl)oxybenzyl cis-2,6-dimethylpiperazine-1-carboxylate was prepared from 2,6-difluoro-4-hydroxybenzyl alcohol, 3-fluorobenzyl chloride and 1-chlorocarbonyl-2,6-dimethyl-4-tert-butoxycarbonylpiperazine according to the methods described for Example 54 and 121 to give the product as a yellow oil: δH (400 MHz; d6-DMSO) 1.13 (6H, d, J 7.0 Hz), 2.60 (2H, dd, J 12, 4.5 Hz), 2.66 (2H, d, J 12 Hz), 3.77–3.86 (2H, m), 5.03 (2H, s), 5.18 (2H, s), 6.84–6.93 (2H, m), 7.16–7.22 (1H, m), 7.27–7.32 (2H, m) and 7.42–7.49 (1H, m); HPLC (XTERRA, 50–80%, 220 nm) 99.8% (5.96 min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07022707B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-f3996aff3ee74aba9b543069427796ae
출처 메모uspto-grants-2006_04