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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 855437생성일: 2026년 10월 24일

1H-Indole-7-carboxylic acid → 1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(ethyl-m-tolyl-amino)-ethyl]-amide

https://huagongshe.com/ko/reaction/855437

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indole-7-carboxylic acidHCID 74281—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물N'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamineHCID 69342865—
용매DichloromethaneHCID 6344—
생성물1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(ethyl-m-tolyl-amino)-ethyl]-amideHCID 8660312059.9%

반응 단계

81 mg (0.50 mol) of 1H-indole-7-carboxylic acid, 162 mg (0.5 mmol) of N′-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamine and 108 mg (0.55 mmol) of EDC.HCl were dissolved in 5 ml DCM. The reaction mixture was stirred at rt over night. The solvent was evaporated and the residue was dissolved in diethyl ether. The organic layer was washed with 1N aqueous HCl solution, once with 1N aqueous NaOH solution and once with saturated aqueous NaCl solution, dried over sodium sulfate, filtered and the solvent was evaporated to leave 140 mg (55%) product as a colorless oil. MS (ISP) 468.4 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259183B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-39ee5e229e144f9586dff008529c1e34
출처 메모uspto-grants-2007_08