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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40090생성일: 2026년 10월 24일

Diisopropylethylamine → 1-Benzyl-N3-(3,4-difluorobenzyl)-N6-(2-hydroxy-2-methylpropyl)-2-isopropyl-1H-indole-3,6-dicarboxamide

https://huagongshe.com/ko/reaction/40090

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-Propanol, 1-amino-2-methyl-HCID 95102—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물1-Benzyl-3-(3,4-difluorobenzylcarbamoyl)-2-isopropyl-1H-indole-6-carboxylic AcidHCID 25060003—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-Benzyl-N3-(3,4-difluorobenzyl)-N6-(2-hydroxy-2-methylpropyl)-2-isopropyl-1H-indole-3,6-dicarboxamideHCID 69226164—

반응 단계

Following General Procedure G, 1-benzyl-3-(3,4-difluorobenzylcarbamoyl)-2-isopropyl-1H-indole-6-carboxylic acid (Compound 56, 35 mg, 0.080 mmol) in DMF (4 ml) was added BOP (40 mg, 0.10 mmol) and DIPEA (20 mg, 0.11 mmol), followed by 1-amino-2-methylpropan-2-ol (10 mg, 0.10 mmol). The reaction was stirred at room temperature for 12 h, diluted with EtOAc, washed with H2O, brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by chromatography on silica gel (5:95 MeOH—CH2Cl2) to yield the title compound as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524917B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0bc62927f45b4da097e030d6b55ab381
출처 메모uspto-grants-2013_09