戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 8732作成日:2026年10月25日

5-(imino-morpholin-4-yl-methyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester → 5-(imino-morpholin-4-yl-methyl)-3,4-dihydro-1H-isoquinoline

https://huagongshe.com/reaction/8732

反応式

関与物質

役割名称HCID仕込み量
反応物5-(imino-morpholin-4-yl-methyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl esterHCID 69595528—
溶媒DichloromethaneHCID 6344—
溶媒Trifluoroacetic acidHCID 6422—
生成物5-(imino-morpholin-4-yl-methyl)-3,4-dihydro-1H-isoquinolineHCID 21983611105.7%

反応手順

5-(Imino-morpholin-4-yl-methyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 27a (0.24 g, 0.69 mmol) was dissolved to room temperature in 10 mL of 10% trifluoroacetic acid in dichloromethane and stirred to room temperature for 18 h. The volatiles were evaporated, the residue was suspended in toluene and evaporated again. The residue was purified by flash chromatography eluting with 7% methanol in dichloromethane containing 0.7% of ammonium hydroxide to yield 0.179 g of 5-(imino-morpholin-4-yl-methyl)-3,4-dihydro-1H-isoquinoline 28a.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091200B2
出典データセットuspto-grants-2006_08
ORD IDord-0008c02400784d04915e7583d17b8539
出典メモuspto-grants-2006_08