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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84836생성일: 2026년 10월 23일

Potassium Carbonate → 4-((1R,2S)-2-aminocyclohexylamino)-5-fluoro-2-(3-methylisothiazol-5-ylamino)benzamide

https://huagongshe.com/ko/reaction/84836

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Binap, (A+-)-HCID 634876—
반응물3-Methylisothiazol-5-ylamine hydrochlorideHCID 2723918—
반응물tert-butyl (1S,2R)-2-(5-bromo-4-cyano-2-fluorophenylamino)cyclohexylcarbamateHCID 69283992—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물4-((1R,2S)-2-aminocyclohexylamino)-5-fluoro-2-(3-methylisothiazol-5-ylamino)benzamideHCID 6928398674.2%

반응 단계

A mixture of tert-butyl (1S,2R)-2-(5-bromo-4-cyano-2-fluorophenylamino)cyclohexylcarbamate (220 mg, 0.534 mmol), 5-amino-3-methylisothiazole hydrochloride (97 mg, 0.644 mmol), BINAP (50 mg, 0.080 mmol), Pd(OAc)2 (35 mg, 0.156 mmol) and K2CO3 (250 mg, 1.81 mmol) in dioxane (4 mL) was degassed with Ar, then was stirred at 120 C for 18 h. After the mixture was filtered, the filtrate was concentrated in vacuo. To a solution of the residue in EtOH (2 mL) and DMSO (0.5 mL), 1N aq. NaOH (0.5 mL) and H2O2 (50% aq., 0.5 mL) were added. After being stirred at room temperature for 3 h, water and EtOAc were added. The organic phase was separated, dried over Na2SO4, concentrated in vacuo. The residue was dissolved in TFA (5 mL). After 30 min of standing, TFA was removed in vacuo. The residue was purified by HPLC to give the titled compound (144 mg). MS 364.4 (M+H); UV 204.7, 292.8 nm

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846928B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-013f73167f30420e8651d731ad198089
출처 메모uspto-grants-2014_09