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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 443262생성일: 2026년 10월 25일

2-(Trifluoromethoxy)benzyl bromide → 4-{5-[4-Methoxymethyl-4-(2-trifluoromethoxybenzyl)-piperidine-1-ylmethyl]-2-methylimidazol-1-ylmethyl}benzonitrile hydrochloride salt

https://huagongshe.com/reaction/443262

반응식

참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethoxy)benzyl bromideHCID 2777254—
반응물1-(4-Cyanobenzyl)-5-chloromethyl-2-methylimidazole hydrochloride saltHCID 21193348—
반응물N-tert-butoxy-carbonyl-4-(2-trifluoromethoxybenzyl)-4-hydroxymethylpiperidineHCID 86754054—
생성물4-{5-[4-Methoxymethyl-4-(2-trifluoromethoxybenzyl)-piperidine-1-ylmethyl]-2-methylimidazol-1-ylmethyl}benzonitrile hydrochloride saltHCID 21193166—

반응 단계

The title compound was prepared using the protocol described in Example 30, Step A-C using 2-(trifluoromethoxy)benzyl bromide in Step B, and in Example 52, Step B-E substituting N-tert-butoxycarbonyl-4-(3-methylbenzyl)-4-hydroxymethylpiperidine with N-tert-butoxy-carbonyl-4-(2-trifluoromethoxybenzyl)-4-hydroxymethylpiperidine in Step B, and substituting 1-(4-cyanobenzyl)-5-chloromethyl-imidazole hydrochloride salt with 1-(4-cyanobenzyl)-5-chloromethyl-2-methylimidazole hydrochloride salt in Step E.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05891889
출처 데이터셋uspto-grants-1999_04
ORD IDord-32f70047ac954a21a0e556edff8b406c
출처 메모uspto-grants-1999_04