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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2067707생성일: 2026년 10월 26일

Potassium Carbonate → 4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-N-o-tolylpyrimidin-2-amine

https://huagongshe.com/reaction/2067707

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tert-butyl 3-(3-trimethylsilylpropynoyl)pyrrolo[3,2-c]pyridine-1-carboxylateHCID 58230463—
반응물HCID 178424377HCID 178424377—
용매2-MethoxyethanolHCID 8019—
생성물4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-N-o-tolylpyrimidin-2-amineHCID 24992386—

반응 단계

173 mg (1.25 mmol) of potassium carbonate are added to a solution of 171 mg (0.50 mmol) of tert-butyl 3-(3-trimethylsilylpropynoyl)pyrrolo[3,2-c]pyridine-1-carboxylate and 265 mg (1.25 mmol) of 2-methylphenylguanidinium nitrate (prepared by the method of J. L. Hughes et al., J. Med. Chem. 1975, 18, 1077-1088) in 2.5 ml of ethylene glycol monomethyl ether, and the mixture is heated at the boil for 18 hours. After cooling, the reaction mixture is partitioned between water and dichloromethane. The organic phase is dried over sodium sulfate and evaporated. The residue is chromatographed on a silica-gel column with dichloromethane/methanol as eluent, giving [4-(1H-pyrrolo-[3,2-c]pyridin-3-yl)pyrimidin-2-yl]-o-tolyl-amine (“A6”) as beige crystals; ESI 303;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08293891B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-0599eb74cc8040f39429083a7082dca9
출처 메모uspto-grants-2012_10