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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294012생성일: 2026년 10월 26일

Triethylamine → 5-(7-benzyloxy-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine

https://huagongshe.com/reaction/2294012

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Amino-5-(chloromethyl)-2-methylpyrimidineHCID 421245—
반응물7-(Benzyloxy)-1,2,3,4-tetrahydroisoquinolineHCID 21463014—
용매DimethylformamideHCID 6228—
생성물5-(7-benzyloxy-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamineHCID 2147368551%

반응 단계

A suspension of 0.23 g (0.0012 mol) of 5-chloromethyl-2-methyl-pyrimidin-4-ylamine in 10 ml of dimethylformamide was treated with 0.42 ml (0.0030 mol) of triethylamine and 0.29 g (0.0012 mol) of 7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline and the mixture was stirred at room temperature under argon for 18 hours. The solvent was distilled off in a high vacuum. The residue was partitioned between dichloromethane/water, extracted and dried over MgSO4. After removing the solvent the residue was chromatographed on silica gel with ethyl acetate as the eluent. 0.22 g (51%) of 5-(7-benzyloxy-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine was obtained as a colourless solid; m.p. 151°-153°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05688798
출처 데이터셋uspto-grants-1997_11
ORD IDord-378920fcdbcd4390a64190d968976ed5
출처 메모uspto-grants-1997_11