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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245744생성일: 2026년 10월 26일

1H-Indole-2-carboxylic acid, 1-methyl- → HCID 178432917, 화합물

https://huagongshe.com/reaction/245744

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indole-2-carboxylic acid, 1-methyl-HCID 27695—
반응물4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
반응물1-methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-indole-2-carboxamideHCID 18450543—
반응물HCID 178432912HCID 178432912—
생성물HCID 178432917HCID 17843291727.9%

반응 단계

Reaction of 1-methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-indole-2-carboxamide (29 mg), prepared from 1-methyl-1H-indole-2-carboxylic acid which was transformed into its acid chloride first and then reacted with 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, and 1-bromo-8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazine (30 mg) according to the procedure described in example 4 step 4c and purification by column chromatography (silica gel; dichloromethane with gradient 0 to 20% of methanol) gave 1-methyl-N-(4-(8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazin-1-yl)phenyl)-1H-indole-2-carboxamide (12 mg)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658794B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-448dea8b6c55473c849f56cd0dd53cd5
출처 메모uspto-grants-2014_02