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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1773414생성일: 2026년 10월 26일

Trifluoroacetic acid → tert-butyl 3-{[(4-{[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]carbamoyl}-3-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]phenyl)amino]methyl}azetidine-1-carboxylate

https://huagongshe.com/reaction/1773414

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Tert-butyl 3-formylazetidine-1-carboxylateHCID 10726182—
반응물Tetramethylammonium Triacetoxyborohydride (>90%)HCID 13696215—
반응물N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-amino-2-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]benzamideHCID 86647628—
용매DichloromethaneHCID 6344—
생성물tert-butyl 3-{[(4-{[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]carbamoyl}-3-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]phenyl)amino]methyl}azetidine-1-carboxylateHCID 86647629—

반응 단계

To a solution of N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-amino-2-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]benzamide (240 mg, 0.42 mmol) in dichloromethane (20 mL) were added tert-butyl 3-formylazetidine-1-carboxylate (116 mg, 0.63 mmol), trifluoroacetic acid (0.32 mL) and tetramethylammonium triacetoxyborohydride (165 mg g, 0.63 mmol). The mixture was stirred at room temperature overnight, then diluted with dichloromethane, washed with NaHCO3 sat.sol. and brine, dried over sodium sulfate and evaporated to dryness.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09255087B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-6dfb40f8ea3a4edfaf0498678d107c0b
출처 메모uspto-grants-2016_02