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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40128생성일: 2026년 10월 24일

Potassium Carbonate → 1-Benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-(1,3-thiazol-2-yloxy)-1H-indole-3-carboxamide

https://huagongshe.com/ko/reaction/40128

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Sodium HydroxideHCID 14798—
반응물2-BromothiazoleHCID 76430—
반응물1-Benzyl-N-(3,4-difluorobenzyl)-6-hydroxy-2-isopropyl-1H-indole-3-carboxamideHCID 25160740—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-Benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-(1,3-thiazol-2-yloxy)-1H-indole-3-carboxamideHCID 59762285—

반응 단계

General Procedure U. To a solution of 1-benzyl-N-(3,4-difluorobenzyl)-6-hydroxy-2-isopropyl-1H-indole-3-carboxamide (Compound 8, 12 mg, 0.028 mmol) in DMF (1 ml) was added K2CO3 (19 mg, 0.14 mmol) and 2-bromothiazole (23 mg, 0.14 mmol). The mixture was stirred at room temperature overnight and a small amount of NaOH was added. The reaction was kept stirring for 72 h, diluted with EtOAc, washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→50% EtOAc-hexanes) to yield the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524917B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-6316f0e3b36a47f98753bbe0910d7f24
출처 메모uspto-grants-2013_09