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HRID 361607作成日:2026年10月26日

Triethylamine → 3,4-Dihydro-N-methoxy-N-methyl-2(1H)-isoquinolinecarboxamide

https://huagongshe.com/reaction/361607

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium CarbonateHCID 10340—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物3,4-Dihydroisoquinoline-2(1H)-carbonyl chlorideHCID 21890571—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物3,4-Dihydro-N-methoxy-N-methyl-2(1H)-isoquinolinecarboxamideHCID 1218591193.5%

反応手順

A solution of 2.73 g of 3,4-dihydro-1H-isoquinoline-2-carbonyl chloride, 55 mg of 4-dimethylamino-pyridine, 1.36 g of N,O-dimethylhydroxylamine hydrochloride and 4.85 ml of triethylamine in 30 ml of methylene chloride was heated to boiling under reflux for 22 h. The reaction mixture was treated at room temperature with 50 ml of a 5% sodium carbonate solution and extracted twice with 50 ml of methylene chloride each time. The combined organic phases were washed once with 50 ml of water and once with 50 ml of a saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The residue was triturated with 50 ml of t-butyl methyl ether, a small amount of insoluble residue was filtered off under suction and the filtrate was concentrated. The residue was dried at room temperature and about 12 mbar. 2.87 g (93%) of 3,4-dihydro-1H-isoquinoline-2-carboxylic acid methoxy-methyl-amide were obtained as an orange oil. MS (EI): 220M30 .

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05866583
出典データセットuspto-grants-1999_02
ORD IDord-08c6d8c75ad94af08228b5173a998f86
出典メモuspto-grants-1999_02