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HRID 491430作成日:2026年10月27日

Quinoxaline-2-carbaldehyde → 2-({4-[2-(4-Tert-butylphenyl)-1,3-benzothiazol-7-yl]piperazin-1-yl}methyl) quinoxaline

https://huagongshe.com/reaction/491430

反応式

関与物質

役割名称HCID仕込み量
反応物Quinoxaline-2-carbaldehydeHCID 594088—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物HCID 57678297HCID 57678297—
触媒Acetic AcidHCID 176—
溶媒1,2-DichloroethaneHCID 11—
生成物2-({4-[2-(4-Tert-butylphenyl)-1,3-benzothiazol-7-yl]piperazin-1-yl}methyl) quinoxalineHCID 1199827755%

反応手順

The piperazine template (0.075 g, 0.213 mmol) of Example 24 was dissolved in 1,2-dichloroethane (3 mL) and treated with quinoxaline-2-carbaldehyde (0.044 g, 0.277 mmol) and glacial acetic acid (2 drops). Sodium triacetoxyborohydride (0.090 g, 0.426 mmol) was added, and the mixture was stirred at room temperature until the reaction was complete by LCMS analysis. The solvent was removed under reduced pressure, and the resulting residue was purified by RP-HPLC to yield the free base (0.0578 g, 55% yield). MS (ESI) m/z 494.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531542B2
出典データセットuspto-grants-2009_05
ORD IDord-e55cb59139414209ac3587dd58e64a21
出典メモuspto-grants-2009_05