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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294008생성일: 2026년 10월 26일

Triethylamine → 2-methyl-5-(6-phenyl-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-pyrimidin-4-ylamine

https://huagongshe.com/reaction/2294008

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6-Phenyl-1,2,3,4-tetrahydroisoquinolineHCID 32396—
반응물5-(Chloromethyl)-2-methylpyrimidin-4-amine--hydrogen chloride (1/1)HCID 21473611—
용매DimethylformamideHCID 6228—
생성물2-methyl-5-(6-phenyl-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-pyrimidin-4-ylamineHCID 986233961%

반응 단계

A suspension of 0.20 g (0.00080 mol) of 5-chloromethyl-2-methyl-pyrimidin-4-ylamine hydrochloride in 10 ml of dimethylformamide was treated with 0.34 ml (0.0024 mol) of triethylamine and 0.19 g (0.00097 mol) of 6-phenyl-1,2,3,4-tetrahydro-isoquinoline and the mixture was stirred at room temperature under argon for 60 hours The mixture was completely freed from the solvents. The residue was partitioned between dichloromethane and water, extracted, chromatographed over silica gel with acetonitrile/methanol 5:1 as the eluent and digested in diethyl ether. 0.16 g (61%) of 2-methyl-5-(6-phenyl-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-pyrimidin-4-ylamine was obtained as white crystals; m.p. 186°-188°. A further 0.03 g of pale yellow crystals was recovered from the mother liquor.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05688798
출처 데이터셋uspto-grants-1997_11
ORD IDord-5c6ec1e12bb3414890f5efa3f07dd982
출처 메모uspto-grants-1997_11