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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15751생성일: 2026년 10월 23일

Hydrazine hydrate (1:1) → benzyl 6-isopropyl-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate

https://huagongshe.com/ko/reaction/15751

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물4-PiperidoneHCID 33721—
반응물Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylateHCID 59342393—
반응물HCID 178418676HCID 178418676—
생성물benzyl 6-isopropyl-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylateHCID 68503449—

반응 단계

5-(4-Chlorophenylsulfonyl)-6-(4-fluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-Benzyl 2-(4-fluorophenyl)-4-oxopiperidine-1-carboxylate, prepared as described for compound 67 in Example using 4-fluorophenylmagnesium bromide, was formylated and treated with hydrazine hydrate as described for compound 50 in Example 1 to give benzyl 6-isopropyl-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate. This compound was then deprotected and treated with 4-chlorophenylsulfonyl chloride followed by NaOH as described for compound 52 in Example 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732609B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ba3ee268dc61420d8103506a34f40fc0
출처 메모uspto-grants-2010_06