戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1274395作成日:2026年10月27日

Sulfuric acid magnesium salt (1:1) → 1-(7-Aza-bicyclo[2.2.1]hept-7-yl)-2-{2-(3,5-dimethylphenyl)-3-[2-(2-pyridin-3-yl-ethylamino)-ethyl]-1H-indol-5-yl)-2-methylpropan-1-one

https://huagongshe.com/reaction/1274395

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Pyridin-3-ylacetaldehydeHCID 11073404—
反応物2-[3-(2-Aminoethyl)-2-(3,5-dimethylphenyl)-1H-indol-5-yl]-1-(7-azabicyclo[2.2.1]hept-7-yl)-2-methyl-propan-1-oneHCID 11761791—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
生成物1-(7-Aza-bicyclo[2.2.1]hept-7-yl)-2-{2-(3,5-dimethylphenyl)-3-[2-(2-pyridin-3-yl-ethylamino)-ethyl]-1H-indol-5-yl)-2-methylpropan-1-oneHCID 2212067151.8%

反応手順

To a solution of 2-[3-(2-aminoethyl)-2-(3,5-dimethylphenyl)-1H-indol-5-yl]-1-(7-aza-bicyclo[2.2.1]hept-7-yl)-2-methylpropan-1-one (183 mg in 10 mL dry chloroform) at 0° C. was added 305 mg magnesium sulfate followed by a solution of 100 mg pyridin-3-yl-acetaldehyde in 1.0 mL chloroform and the mixture stirred at low temperature. After 6 minutes, a solution of 52 mg sodium cyanoborohydride in 0.80 mL methanol was added and the pH djusted to pH6 by the addition of 10% acetic acid in methanol. After 30 minutes, the reaction was quenched by the addition of saturated sodium bicarbonate and the mixture extracted with ethyl acetate. The organic portion was washed successively with saturated ammonium chloride, sodium bicarbonate and brine, then dried over sodium sulfate. Purification of the concentrate by flash chromatography on silica gel (methylene chloride:methanol, 93:7; then 88:12) gave the title compound (118 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06156767
出典データセットuspto-grants-2000_12
ORD IDord-bbaed464558f4d438530e040e59f2e33
出典メモuspto-grants-2000_12