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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1182709생성일: 2026년 10월 27일

Sodium Bicarbonate → N-(3-((2-butyl-1-oxoisoindolin-5-ylamino)methyl)pyridin-4-yl)pivalamide

https://huagongshe.com/reaction/1182709

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물N-(3-formylpyridin-4-yl)-2,2-dimethylpropanamideHCID 2779664—
반응물Sodium borohydrideHCID 4311764—
반응물5-Amino-2-butyl-2,3-dihydro-1H-isoindol-1-oneHCID 67432065—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물N-(3-((2-butyl-1-oxoisoindolin-5-ylamino)methyl)pyridin-4-yl)pivalamideHCID 67434684—

반응 단계

5-Amino-2-butylisoindolin-1-one (49.5 mg, 0.242 mmol) was added to a solution of N-(3-formylpyridin-4-yl)pivalamide (50 mg, 0.242 mmol) in acetic acid (1 mL). After stiffing for 5 days, water and sat aqueous NaHCO3 solution were added. The mixture was extracted with EtOAc, the combined organic layers were washed with water, dried over MgSO4 and the solvent was removed in vacuo. The residue obtained was dissolved in MeOH (3 mL) and NaBH4 (18.3 mg, 0.485 mmol) was added. After stirring overnight, water and sat. aqueous NaHCO3 solution were added. Extraction with EtOAc, washing of the combined organic layers with water and drying over MgSO4 provided the crude product which was purified by HPLC (24 mg, 19%). ESI-MS [M+H]+=395.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08664214B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-46160462a979401a929b3686ce488800
출처 메모uspto-grants-2014_03