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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602142생성일: 2026년 10월 25일

1-Boc-3-hydroxypiperidine → 1-(tert-Butoxycarbonyl)-3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]methoxy]piperidine

https://huagongshe.com/reaction/602142

반응식

참여 물질

역할이름HCID투입량
반응물1-Boc-3-hydroxypiperidineHCID 545699—
반응물5-(Chloromethyl)-2-(4-chlorophenyl)-4-methyl-1,3-thiazoleHCID 2763694—
생성물1-(tert-Butoxycarbonyl)-3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]methoxy]piperidineHCID 5757214044.2%

반응 단계

Using 1-(tert-butoxycarbonyl)-3-hydroxypiperidine (201 mg, 1.00 mmol) and 5-chloromethyl-2-(4-chlorophenyl)-4-methylthiazole (258 mg, 1.00 mmol), the same procedure was followed as in Step 5a of Example 5 to give 187 mg (44%) of the desired compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902367B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-6fcabbb6b52b4193a2399ef056a7b722
출처 메모uspto-grants-2011_03