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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 361607생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/361607

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium CarbonateHCID 10340—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물3,4-Dihydroisoquinoline-2(1H)-carbonyl chlorideHCID 21890571—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물3,4-Dihydro-N-methoxy-N-methyl-2(1H)-isoquinolinecarboxamideHCID 1218591193.5%

반응 단계

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 .

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05866583
출처 데이터셋uspto-grants-1999_02
ORD IDord-08c6d8c75ad94af08228b5173a998f86
출처 메모uspto-grants-1999_02