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HRID 1624307作成日:2026年10月27日

1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanal → 2-[4-(4-Methoxy-5,6,7,8-tetrahydroquinolin-8-ylamino)-butyl]-isoindole-1,3-dione

https://huagongshe.com/reaction/1624307

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4-Methoxy-5,6,7,8-tetrahydroquinolin-8-amineHCID 22018617—
溶媒DichloromethaneHCID 6344—
生成物2-[4-(4-Methoxy-5,6,7,8-tetrahydroquinolin-8-ylamino)-butyl]-isoindole-1,3-dioneHCID 6917879054.4%

反応手順

Using General Procedure B: Reaction of 8-amino-4-methoxy-5,6,7,8-tetrahydroquinoline (0.297 g, 1.67 mmol) and 4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-butyraldehyde (0.371, 1.71 mmol) with NaBH(OAc)3 (0.493 g, 2.33 mmol) in CH2Cl2 (8 mL) for 60 minutes followed by purification of the crude material by column chromatography on silica gel (20:1 CH2Cl2—CH3OH) provided 0.345 g (54%) of 2-[4-(4-Methoxy-5,6,7,8-tetrahydro-quinolin-8-ylamino)-butyl]-isoindole-1,3-dione as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08778967B2
出典データセットuspto-grants-2014_07
ORD IDord-0840b44d153f49e0ae56d128557489e8
出典メモuspto-grants-2014_07