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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72463생성일: 2026년 10월 24일

Potassium Carbonate → 2-(3-(3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)phenoxy)azetidin-1-yl)-5-chloronicotinic acid

https://huagongshe.com/ko/reaction/72463

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Sodium HydroxideHCID 14798—
반응물tert-Butyl 4-(3-hydroxyphenyl)piperazine-1-carboxylateHCID 18669061—
반응물Methyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinateHCID 86697874—
용매DimethylformamideHCID 6228—
생성물2-(3-(3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)phenoxy)azetidin-1-yl)-5-chloronicotinic acidHCID 67958153—

반응 조건

온도120 °C

반응 단계

To a solution of tert-butyl 4-(3-hydroxyphenyl)piperazine-1-carboxylate (D18) (143.18 mg, 0.514 mmole) in dimethylformamide (2 ml), potassium carbonate (71 mg, 0.514 mmol) and the reaction mixture was heated 2 h at 80° C. methyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinate (D63) (150 mg, 0.467 mmol) in dimethylformamide (2 ml) was added dropwise and the resulting mixture stirred 21 h at 120° C. After cooling at room temperature, 1M NaOH (0.935 ml) was added and the mixture stirred 1 h at 120° C. After cooling the reaction mixture was extracted with diethylether (2×10 ml) and the aqueous was evaporated in vacuo. The residue was purified by SPE-Si cartridge (5 g) eluting with a mixture dichloromethane/methanol from 100/0 to 80/20. Collected fractions, after solvent evaporation afforde the title compound (D110) (155 mg)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828987B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-cc660e40c4514ed698b84628d03b181e
출처 메모uspto-grants-2014_09