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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605696생성일: 2026년 10월 26일

Formaldehyde → 1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)-N-methylazetidin-3-amine

https://huagongshe.com/reaction/605696

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물MethanolHCID 887—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1-({3,4-Difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amineHCID 16221889—
용매TetrahydrofuranHCID 8028—
생성물1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)-N-methylazetidin-3-amineHCID 1622260535.9%

반응 단계

To a solution of 1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amine (0.10 M in acetonitrile, 1.0 mL, 0.09 mmol), prepared using procedures similar to those described in Example 2, in 1:1 ratio of methanol and tetrahydrofuran (2.0 mL) was added formaldehyde (37% wt, 6.7 μL, 0.09 mmol) followed by sodium cyanoborohydride (11.0 mg, 0.18 mmol). The reaction mixture was stirred at room temperature for 16 h, at which time it was quenched with saturated aqueous ammonium chloride. The solution was then purified directly by reverse phase HPLC to afford the title compound (14.9 mg). 1H NMR (400 MHz, CDCl3): 8.13 (br s, 1H), 7.35 (d, 1H), 7.30 (d, 1H), 7.09-7.04 (m, 1H), 6.84-6.78 (m, 1H), 6.60-6.54 (m, 1H), 4.46-4.33 (br m, 4H), 3.93 (br m, 1H), 2.64 (s, 3H). MS (EI) for C17H15F3IN3O: 462 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915250B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-7d67ac174ee647aba5c17b77b53eb739
출처 메모uspto-grants-2011_03