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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1794096생성일: 2026년 10월 27일

Benzenemethanol, 4-(difluoromethoxy)-2,6-difluoro- → 2,6-Difluoro-4-difluoromethoxybenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride

https://huagongshe.com/reaction/1794096

반응식

참여 물질

역할이름HCID투입량
반응물Benzenemethanol, 4-(difluoromethoxy)-2,6-difluoro-HCID 69140944—
반응물rel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylateHCID 86585999—
생성물2,6-Difluoro-4-difluoromethoxybenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochlorideHCID 69141564—

반응 단계

2,6-Difluoro-4-difluoromethoxybenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride was prepared from cis 1-chlorocarbonyl-2,6-dimethyl-4-tert-butoxycarbonylpiperazine and 2,6-difluoro-4-difluoromethoxybenzyl alcohol according to the method described for Example 54 to give the product as a, white solid (0.1406 g, 65% overall); νmax (nujol)/cm−1 3342, 1684, 1640, 1599, 1378, 1308, 1166, and 1089; δH (400 MHz, DMSO-d6) 9.69 (2H, br), 7.38 (1H, t, J 73 Hz), 7.15–7.10 (2H, m), 5.14 (2H, s), 4.24 (2H, m), 3.13 (2H, d, J 13 Hz), 3.05 (2H, dd, J 5.2 and 13 Hz), and 1.27 (6H, d, J 7.2 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07022707B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-b63c0ea28f5e4419963531ed084e00a7
출처 메모uspto-grants-2006_04