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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133107생성일: 2026년 10월 26일

Sodium triacetoxyborohydride → 2-(4-(1,1-Dimethylethyl)phenyl)-8-((1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)amino)-1(2H)-phthalazinone

https://huagongshe.com/reaction/133107

반응식

참여 물질

역할이름HCID투입량
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
반응물8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-oneHCID 69160627—
용매DichloromethaneHCID 6344—
생성물2-(4-(1,1-Dimethylethyl)phenyl)-8-((1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)amino)-1(2H)-phthalazinoneHCID 11625993—

반응 단계

To a solution of 8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-one (Example 1, Step E, 0.36 g, 1.1 mmol, 1 eq) and CH2Cl2 (50 mL) was added 1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (0.16 g, 1.1 mmol, 1 eq) and NaBH(OAc)3 (0.72 g, 3.4 mmol, 3.0 eq). The reaction was stirred at RT for 12 h then quenched with H2O and extracted with CH2Cl2. The organic layer was washed with H2O and brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by silica flash chromatography (10-75% EtOAc:hexane) to give the desired product as a yellow solid. MS m/e 424 (M+H)+. Calc'd for C26H25N5O-423.51.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390820B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-27cc4fb6d8be4f56838139a945ac0d5d
출처 메모uspto-grants-2008_06