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HRID 394457作成日:2026年10月26日

1-Bromo-3-chloropropane → 2-(3-Chloropropyl)-7-(morpholin-4-ylsulfonyl)-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/394457

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物TriethylamineHCID 8471—
反応物7-(Morpholine-4-sulfonyl)-1,2,3,4-tetrahydroisoquinolineHCID 21983663—
溶媒DimethylformamideHCID 6228—
生成物2-(3-Chloropropyl)-7-(morpholin-4-ylsulfonyl)-1,2,3,4-tetrahydroisoquinolineHCID 1817651146%

反応条件

温度40 °C

反応手順

1.2 g (4.4 mmol) of 7-(morpholin-4-ylsulfonyl)-1,2,3,4-tetra-hydroisoquinoline and 1.0 g (10 mmol) of triethylamine were dissolved in DMF at 40° C., 1.1 g (6.6 mmol) of 1-bromo-3-chloropropane were added dropwise, and the mixture was stirred at 40° C. for 3 h. For workup, the mixture was concentrated, and the residue was taken up in water and extracted with methyl tert-butyl ether. Drying over sodium sulfate, filtration and removal of the solvent were followed by purification by chromatography (silica gel; mobile phase: methylene chloride with 2% methanol) to afford 0.7 g (2 mmol) of a pale oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06602867B1
出典データセットuspto-grants-2003_08
ORD IDord-47ac1345935440fc89bfcfc31a7fbf21
出典メモuspto-grants-2003_08