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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921765생성일: 2026년 10월 25일

Acetic Acid → 2-((2-Chloro-5-cyano-3-((4-(methylsulfonyl)piperazin-1-yl)methyl)phenyl)amino)-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile

https://huagongshe.com/reaction/921765

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Trimethyl orthoformateHCID 9005—
반응물Sodium BicarbonateHCID 516892—
반응물1-(Methylsulfonyl)piperazineHCID 709161—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물2-((2-Chloro-5-cyano-3-formylphenyl)amino)-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrileHCID 86708648—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물2-((2-Chloro-5-cyano-3-((4-(methylsulfonyl)piperazin-1-yl)methyl)phenyl)amino)-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrileHCID 8670865031.2%

반응 단계

A solution of 2-((2-chloro-5-cyano-3-formylphenyl)amino)-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (Example 400) (18 mg, 0.048 mmol), 1-(methylsulfonyl)piperazine (9.5 mg, 0.058 mmol), trimethylorthoformate (0.027 mL, 0.242 mmol), and acetic acid (3 μL, 0.05 mmol) in a mixture of MeOH (0.5 mL) and DCM (0.5 mL) was stirred at room temperature for 15 min. A solution of sodium cyanoborohydride (0.097 mL, 1M in THF mL, 0.097 mmol) was added and the reaction was left stirring at room temperature overnight. Additional sodium cyanoborohydride (0.097 mL, 1M in THF mL, 0.097 mmol) was added and the reaction was left stirring for 1 day. A saturated aq. solution of NaHCO3 solution was added and, after 15 min, this was extracted with a mixture of 5% MeOH in DCM (5×). The combined organic extracts were dried with sodium sulfate and the solvent was removed. Silica gel radial chromatography of the residue eluting with DCM containing 0 to 2% MeOH afforded the title compound (7.9 mg) as foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273057B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-8e08c63474f046728e9f5eb23e60a56d
출처 메모uspto-grants-2016_03