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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1518372생성일: 2026년 10월 27일

1-Phenylpiperazine → 3-(4-Methylpiperazin-1-yl)phenol

https://huagongshe.com/reaction/1518372

반응식

참여 물질

역할이름HCID투입량
반응물1-PhenylpiperazineHCID 7096—
반응물1-(3-Hydroxyphenyl)piperazineHCID 2736597—
반응물methyl 2-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-5-((4-phenylpiperazin-1-yl)methyl)thiazole-4-carboxylateHCID 59447670—
반응물HCID 178499107HCID 178499107—
생성물3-(4-Methylpiperazin-1-yl)phenolHCID 11011455—

반응 단계

Compound 87A was prepared in a similar manner to the synthesis of compound 62A by substituting compound 45C and phenylpiperazine with paraformahyde and 3-(piperazin-1-yl)phenol, respectively: 1H NMR (DMSO-d6): δ 9.07 (s, 1H), 6.94-6.98 (m, 1H), 6.36 (d, J=8.13, 2.4 Hz, 2H), 8.28-8.29 (m, 1H), 6.18-6.21 (m, 1H), 3.04-3.07 (m, 4H), 2.41-2.43 (m, 4H), 2.21 (s, 3H). ESI (+)/MS: 193 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08232273B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-1db435a09d5f493fa91f3a03b4cfc019
출처 메모uspto-grants-2012_07