戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 41567作成日:2026年10月23日

Acetic Acid → tert-butyl 4-allyl-4-((1-tosyl-1H-indol-3-yl)methylamino)piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/41567

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium BicarbonateHCID 516892—
反応物1-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehydeHCID 735817—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物741687-08-1HCID 67287394—
溶媒1,2-DichloroethaneHCID 11—
生成物tert-butyl 4-allyl-4-((1-tosyl-1H-indol-3-yl)methylamino)piperidine-1-carboxylateHCID 6725278160.1%

反応条件

温度60 °C

反応手順

To a solution of 1-tosyl-1H-indole-3-carbaldehyde [50562-79-3] (1.90 g, 6.35 mmol) in 1,2-dichloroethane (30 mL) were added tert-butyl 4-allyl-4-aminopiperidine-1-carboxylate [741687-08-1] (1.52 g, 6.35 mmol) and acetic acid (381 mg, 6.35 mmol). The resulting solution was heated at 60° C. for 3 h. Then NaBH(OAc)3 was added and the reaction mixture was heated at 60° C. for 38 h. The mixture was cooled to rt, saturated NaHCO3 solution (30 mL) was added and extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with water and brine, then dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude mixture was purified by flash-column chromatography over silicagel (eluent: 20% ethyl acetate/hexane) to yield the title compound (2.0 g, 60%). [LCMS RtE=0.34 min, [M+H]+=524.0]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530648B2
出典データセットuspto-grants-2013_09
ORD IDord-f507aec85ad84e9ca7dc89d2e278bfa1
出典メモuspto-grants-2013_09