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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1481539생성일: 2026년 10월 26일

5-tert-butyl-4-chloro-2-methyl-2H-pyrazole-3-carboxylic acid [2-methoxy-3-nitro-6-(2-trifluoromethyl-phenyl)-pyridin-4-yl]-amide → HCID 178494020, 화합물

https://huagongshe.com/reaction/1481539

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참여 물질

역할이름HCID투입량
반응물5-tert-butyl-4-chloro-2-methyl-2H-pyrazole-3-carboxylic acid [2-methoxy-3-nitro-6-(2-trifluoromethyl-phenyl)-pyridin-4-yl]-amideHCID 67411653—
촉매IronHCID 23925—
용매Acetic AcidHCID 176—
생성물HCID 178494020HCID 178494020—

반응 조건

온도100 °C

반응 단계

A solution of 5-tert-butyl-4-chloro-2-methyl-2H-pyrazole-3-carboxylic acid [2-methoxy-3-nitro-6-(2-trifluoromethyl-phenyl)-pyridin-4-yl]-amide (149 mg, 0.291 mmol, prepared as described in STEP A above) in AcOH (10 mL) was treated with iron powder (81.3 mg, 1.46 mmol), and the resulting mixture was heated to 100° C. for 1.5 h. The cooled mixture was concentrated in vacuo, taken up in saturated aqueous NaHCO3 (50 mL), and extracted twice with EtOAc (40 mL). The combined organic extracts were dried over MgSO4 and concentrated in vacuo. The residue was purified on a 12-g SEPRA Si 50 SPE column (Flow rate=15 mL/min; Eluent=EtOAc-hexanes, 1:99 for 10 min, then 1:99 to 1:4 over 40 min) to yield 2-(5-tert-butyl-4-chloro-2-methyl-2H-pyrazol-3-yl)-4-methoxy-6-(2-trifluoromethyl-phenyl)-3H-imidazo[4,5-c]pyridine as a white solid. Mass Spectrum (LCMS, ESI pos.): Calculated for C22H21N5OClF3: 464.1 (M+H). Measured: 464.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409915B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-89fe2f4773af41c7a134929bf57a8b17
출처 메모uspto-grants-2016_08