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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1853294생성일: 2026년 10월 26일

1,8-Diazabicyclo(5.4.0)undec-7-ene → Methyl 6-methylisoquinoline-3-carboxylate

https://huagongshe.com/reaction/1853294

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참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물SodiumHCID 5360545—
반응물Methyl 2-acetamido-2-(dimethoxyphosphoryl)acetateHCID 11746707—
반응물4-(Dimethoxymethyl)pyridine-3-carbaldehydeHCID 86673065—
용매DichloromethaneHCID 6344—
생성물Methyl 6-methylisoquinoline-3-carboxylateHCID 2224364462.7%

반응 조건

온도0 °C

반응 단계

To a cold solution of 4-Dimethoxymethyl-pyridine-3-carbaldehyde (tetrahedron letters 2004 (45), 553-556) (400 mg, 1.91 mmol) in dichloromethane (10 ml) was slowly added a solution of Acetylamino-(dimethoxy-phosphoryl)-acetic acid methyl ester (synthesis 1984, 53-60) (503 mg, 2.1 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.31 ml, 2.1 mmol). The solution was stirred at 0° C. for 1 hour then at room temperature for 18 hours. The mixture was poured onto a cold saturated solution of sodium hydrogenocarbonate, extracted with dichloromethane, dried over sodium sulfate and concentrated to dryness. The residue was dissolved in toluene (49 ml) and treated with p-toleunesulfonic acid (315 mg, 1.66 mmol). The mixture was heated at reflux temperature for 18 hours and then concentrated under vacuum. The brown residue was dissolved in ethyl acetate, washed with a saturated solution of sodium hydrogenocarbonate, brine, dried over sodium sulfate and concentrated to yield methyl 6-methyl-isoquinoline-3-carboxylate (241 mg, 62%) as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962627B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-9472ff5011434884ad2bdd85d6a2b29c
출처 메모uspto-grants-2015_02