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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229400생성일: 2026년 10월 25일

Phenol → 2-Phenoxypyrimidine

https://huagongshe.com/reaction/229400

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물SulfonylpyrimidineHCID 18369498—
생성물2-PhenoxypyrimidineHCID 5324768—

반응 단계

In step 1 of Scheme A, sulfanylpyrimidine compound a is treated with peracid or like oxidizing agent to afford sulfonylpyrimidine b. In step 2, sulfonylpyrimidine b is reacted with phenol compound c in the presence of base to provide phenoxypyrimidine compound d. Phenoxypyrimidine d is then treated with hydrazine in step 3 to yield hydrazinopyrimidine compound e. In step 4, hydrazinopyrimidine compound e undergoes a cyclization under basic conditions to afford a pyrazolone compound f. In step 5 the pyrazolone compound f is protected under basic conditions to give a protected pyrazol compound g. Partial deprotection of compound g in step 6 affords pyrazol compound h. In step 7 pyrazol compound h is reacted with alkylating agent i to give pyrazol ester compound j. In step 8 pyrazol ester i is deprotected to give a compound of formula II in accordance with the invention.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07563800B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-1587df9371954d788d0ee4da81d0c283
출처 메모uspto-grants-2009_07