돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097838생성일: 2026년 10월 27일

Triethylamine → 1-{1-[6-Chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carbonyl]-piperidin-4-yl}-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1097838

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물1-Piperidin-4-yl-1,3-dihydro-2H-indol-2-oneHCID 2761152—
반응물6-Chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carboxylic acidHCID 59756704—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-{1-[6-Chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carbonyl]-piperidin-4-yl}-1,3-dihydro-indol-2-oneHCID 2498765648.4%

반응 단계

To a suspension of 0.10 g (0.31 mmol) 6-chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carboxylic acid and one drop of DMF in 2 ml dichloromethane were added dropwise at 0° C. 0.032 ml (0.37 mmol) oxalyl chloride. The mixture was allowed to warm to room temperature, stirred for 1 h and subsequently added dropwise to a solution of 74 mg (0.34 mmol) 1-piperidin-4-yl-1,3-dihydro-indol-2-one and 63 mg (0.62 mmol) triethylamine in 1 ml dichloromethane at room temperature. After stirring over night the reaction mixture was concentrated and the residue was purified by flash chromatography to give 78 mg (48%) of the title compound as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143281B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-455b4d338d37435a8cbcdc0837e5a105
출처 메모uspto-grants-2012_03