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HRID 1193398作成日:2026年10月27日

Binap, (A+-)- → HCID 66799007、化合物

https://huagongshe.com/reaction/1193398

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4-N-Boc-4-N-Methyl-aminopiperidineHCID 2756806—
反応物2-Chloro-6-methylpyrazineHCID 7170095—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物HCID 66799007HCID 6679900747%

反応手順

KOBut (483 mg, 4.32 mmol, 2.5 eq) was added at room temperature to a solution of tert-butyl methyl(piperidin-4-yl)carbamate (stage 3 AMN-60) (370 mg, 1.72 mmol, 1 eq) and 2-chloro-6-methylpyrazine (244 mg, 1.9 mmol, 1.1 eq) in toluene (50 ml) and the mixture was degassed for 30 min with argon. BINAP (64.5 mg, 0.103 mmol, 0.06 eq) and Pd2(dba)3 (31.6 mg, 0.034 mmol, 0.02 eq) were added and the reaction mixture was refluxed for 16 h. After cooling, concentration under reduced pressure was carried out. The residue was taken up in dichloromethane (50 ml) and washed with water (30 ml) and saturated sodium chloride solution (30 ml) and dried over sodium sulfate. The solvent was removed by distillation under reduced pressure and the crude product so obtained was purified by column chromatography (Alox, 0.5% methanol/dichloromethane). The desired product was in the form of a brown solid. Yield: 47% (250 mg, 0.816 mmol)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08680159B2
出典データセットuspto-grants-2014_03
ORD IDord-a1044dc86d6d4014993a32f2ef429826
出典メモuspto-grants-2014_03