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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 514393생성일: 2026년 10월 25일

Methyl 4-(4-methylphenyl)-2,4-dioxobutanoate → methyl 1-(4-cyanopyridin-2-yl)-5-(4-methylphenyl)-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/514393

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-(4-methylphenyl)-2,4-dioxobutanoateHCID 308119—
반응물2-Hydrazinylpyridine-4-carbonitrile hydrochloride saltHCID 86725484—
용매Acetic AcidHCID 176—
생성물methyl 1-(4-cyanopyridin-2-yl)-5-(4-methylphenyl)-1H-pyrazole-3-carboxylateHCID 8672551985%

반응 단계

A solution of methyl 4-(4-methylphenyl)-2,4-dioxobutanoate (500 mg, 22.7 mmol) and 2-hydrazinylpyridine-4-carbonitrile hydrochloride salt (500 mg, 24.2 mmol, PREPARATION 3) in AcOH (10 mL) was heated at 100° C. for 30 min and cooled to rt. The solution was concentrated to an oily residue which was partitioned between EtOAc (50 mL) and water (50 mL). The pH was adjusted to pH=8 using a saturated aq. Na2CO3 solution. The organics were dried (MgSO4), filtered, and concentrated to give a solid which was triturated with MTBE/hexanes (1:1) and filtered to give the title compound (613 mg, 85%) as a yellow solid. 1H NMR (400 MHz, CD3OD): δ 2.48 (3H, s), 3.92 (3H, s), 7.01 (1H, s), 7.08-7.21 (4H, m), 7.71 (1H, d, J=4.8 Hz), 8.12 (1H, s), 8.48 (1H, d, J=4.8 Hz), 8.00 (1H, s), 8.48 (1H, d, J=8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09107916B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-9200489db5bb4663af329ed15a58889a
출처 메모uspto-grants-2015_08