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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218495생성일: 2026년 10월 25일

2-((Tert-butyldimethylsilyl)oxy)acetaldehyde → 3-[2-(Tert-butyl-dimethyl-silanyloxy)-ethylamino]-5-(3,5-dicyano-2,6-dimethyl-1,4-dihydro-pyridin-4-yl)-indazole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/218495

반응식

참여 물질

역할이름HCID투입량
반응물2-((Tert-butyldimethylsilyl)oxy)acetaldehydeHCID 4187788—
반응물tert-Butyl 3-amino-5-(3,5-dicyano-2,6-dimethyl-1,4-dihydropyridin-4-yl)-1H-indazole-1-carboxylateHCID 24959832—
생성물3-[2-(Tert-butyl-dimethyl-silanyloxy)-ethylamino]-5-(3,5-dicyano-2,6-dimethyl-1,4-dihydro-pyridin-4-yl)-indazole-1-carboxylic acid tert-butyl esterHCID 69044121—

반응 단계

3-Amino-5-(3,5-dicyano-1,4-dihydro-2,6-dimethyl-4-pyridinyl)-1H-indazole-1-carboxylic acid tert-butyl ester (16.1 g, 41.23 mmol), from Synthetic Example 18, was reacted with (tert-butyl-dimethyl-silanyloxy)-acetaldehyde (CAS 102191-92-4, obtained from Aldrich, 10.06 g, 58 mmol), according to the procedure detailed in Synthetic Example 19. The crude 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethylamino]-5-(3,5-dicyano-2,6-dimethyl-1,4-dihydro-pyridin-4-yl)-indazole-1-carboxylic acid tert-butyl ester thus obtained was used without further purification in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198456B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-2b10b8345ae8481b9784f34845a00e48
출처 메모uspto-grants-2012_06