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HRID 133107作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
反応物8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-oneHCID 69160627—
溶媒DichloromethaneHCID 6344—
生成物2-(4-(1,1-Dimethylethyl)phenyl)-8-((1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)amino)-1(2H)-phthalazinoneHCID 11625993—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390820B2
出典データセットuspto-grants-2008_06
ORD IDord-27cc4fb6d8be4f56838139a945ac0d5d
出典メモuspto-grants-2008_06