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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 906623생성일: 2026년 10월 26일

Lithium Chloride → 2-Amino-5-pyrazin-2-yl-4-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/906623

반응식

참여 물질

역할이름HCID투입량
반응물Lithium ChlorideHCID 433294—
반응물2-(Tributylstannyl)pyrazineHCID 2737316—
반응물Phenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
반응물Methyl 2-amino-5-iodo-4-(trifluoromethyl)benzoateHCID 53436880—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물2-Amino-5-pyrazin-2-yl-4-trifluoromethyl-benzoic acid methyl esterHCID 1196578238.4%

반응 조건

온도120 °C

반응 단계

A solution containing 2-amino-5-iodo-4-trifluoromethyl-benzoic acid methyl ester (750 mg, 2.17 mmol), 2-tributylstannylpyrazine (1.0 g, 2.7 mmol) and (Ph3P)4Pd (125.6 mg, 0.109 mmol) in dioxane (40 mL) was heated at 120° C. for 17 h. LiCl (276.4 mg, 6.5 mmol) was added and the reaction mixture was refluxed for 1.5 h prior to the addition of di-t-butyl-p-cresol (188 mg, 0.85 mmol) and another portion of (Ph3P)4Pd (251.2 mg, 0.22 mmol). Heating was continued for 16 h, for a total reaction time of 36 h. After cooling to r.t., the solvent was removed in vacuo and the residue was purified by flash chromatography (200 g silica gel, hexanes→EtOAc:hexanes (3:7 to 1:1)). The fractions containing the product were combined and concentrated in vacuo. The resultant oil was further purified by partioning between CH3CN and hexanes. The acetonitrile layer was concentrated in vacuo to furnish the title compound (248 mg, 38%) as a solid. API-ES: m/z 298 [M+H]+, rt 4.18 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08012988B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-b3f596651e644fb2bf07956801352832
출처 메모uspto-grants-2011_09