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HRID 251079作成日:2026年10月26日

1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanal → 2-[4-(1-Methyl-1-pyridin-2-yl-ethylamino)-butyl]-isoindole-1,3-dione

https://huagongshe.com/reaction/251079

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanalHCID 77150—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-(2-Pyridyl)-2-propylamineHCID 22736922—
生成物2-[4-(1-Methyl-1-pyridin-2-yl-ethylamino)-butyl]-isoindole-1,3-dioneHCID 67273132—

反応手順

Using General Procedure B, reaction of 1-methyl-1-pyridin-2-yl-ethylamine (Chakravarty, P K et al. Bioorg. Med. Chem. Lett. 2003, 13, 147-150) with 4-(1,3-Dioxo-1,3-dihydroisoindole-2-yl)-butyraldehyde and NaBH(OAc)3 gave 2-[4-(1-methyl-1-pyridin-2-yl-ethylamino)-butyl]-isoindole-1,3-dione as a colorless oil. 1H NMR (CDCl3) δ 1.46 (s, 6H), 1.50-1.56 (m, 2H), 1.60-1.74 (m, 2H), 2.31 (t, 2H, J=7.0 Hz), 3.65 (t, 2H, J=7.1 Hz), 7.07-7.14 (m, 1H), 7.39 (d, 1H, J=8.3 Hz), 7.63 (td, 1H, J=7.7, 1.8 Hz), 7.66-7.74 (m, 2H), 7.77-7.87 (m, 2H), 8.56 (d, 1H, J=3.9 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863293B2
出典データセットuspto-grants-2011_01
ORD IDord-488a270a3b5a4ec6b76c36d8eabeddb2
出典メモuspto-grants-2011_01