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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 855369생성일: 2026년 10월 24일

1H-Indole-7-carboxylic acid → 1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-difluoromethoxy-phenyl)-ethyl]-amide

https://huagongshe.com/ko/reaction/855369

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indole-7-carboxylic acidHCID 74281—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물(4-Tert-butyl-benzyl)-[2-(4-difluoromethoxy-phenyl)-ethyl]-amineHCID 69341978—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-difluoromethoxy-phenyl)-ethyl]-amideHCID 8660307379.7%

반응 단계

To a solution of 48 mg (0.3 mmol) of 1H-indole-7-carboxylic acid and 96 mg of TBTU (0.3 mmol) in 3 ml DMF, were added 0.26 ml (1.5 mmol) of N,N-diisopropylethyl amine. After stirring for 5 min at rt, 105 mg (0.3 mmol) of (4-tert-butyl-benzyl)-[2-(4-difluoromethoxy-phenyl)-ethyl]-amine in 2 ml DMF were added. After 2.5 h stirring at rt, the reaction mixture was diluted with 50 ml water and extracted with 2×50 ml EtOAc. The combined organic phases were washed with water and brine, dried with magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (8 g silica gel; EtOAc/heptane 1:6) to give 114 mg white solid (68%). MS (ISP) 477.4 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259183B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-ff67d4d3026f4a0c895336259d14b3f6
출처 메모uspto-grants-2007_08