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HRID 1803514作成日:2026年10月25日

Binap, (A+-)- → 4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1803514

反応式

関与物質

役割名称HCID仕込み量
反応物Binap, (A+-)-HCID 634876—
反応物3-Piperidin-1-ylmethyl-benzylamineHCID 2794678—
反応物Sodium t-butoxideHCID 23676156—
反応物6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-oneHCID 58447352—

反応手順

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (70 mg, 0.27 mmol), 3-piperidin-1-ylmethyl-benzylamine (72 mg, 0.35 mmol), Pd2(dba)3 (25 mg, 0.027 mmol), rac-BINAP (51 mg, 0.081 mmol) and NaOt-Bu (76 mg, 0.81 mmol) in DMA (6 mL) was heated at 80° C. for 1 h. The mixture was allowed to cool, diluted with EtOAc (25 mL) and washed with water (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/hexanes) yielded the title compound. 4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-one: 16 mg (15.5%): m/z (M+H)=383. 1H-NMR (DMSO-d6) δ: 12.30 (s, 1H), 7.95 (d, 1H), 7.63 (m, 1H), 7.25 (m, 3H), 7.15 (m, 2H), 6.75 (s, 1H), 4.41 (d, 2H), 3.37 (s, 2H), 2.24 (m, 4H), 1.38 (m, 4H), 1.32 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08349836B2
出典データセットuspto-grants-2013_01
ORD IDord-057e39f9dafb4b95bea5b57b87c12f9e
出典メモuspto-grants-2013_01