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HRID 374986생성일: 2026년 10월 25일

Formaldehyde → 4-bis(phenylmethyl)amino-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-2-methanol

https://huagongshe.com/reaction/374986

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Acetone cardiceHCID 18522661—
반응물N,N-bis(phenylmethyl)-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 18995666—
반응물Carbontetrachloride dry-iceHCID 86602444—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-bis(phenylmethyl)amino-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-2-methanolHCID 18995665—

반응 단계

Butyllithium (1.6 mL of 2.5M in hexanes, 4 mmole) was added to a chilled (dry ice/acetone bath) solution of N,N-bis(phenylmethyl)-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine (1.7 g, 4 mmole) in tetrahydrofuran. No color change was observed. The reaction mixture was warmed to -20° C. (dry ice/carbon tetrachloride) and the reaction turned red in color. Formaldehyde gas entrained in a flow of nitrogen was added to the reaction mixture. After several minutes the reaction turned to a solid mass and the ice bath was removed. The reaction mixture was allowed to warm to ambient temperature and the color of the reaction mixture changed from red to yellow. The reaction was diluted with diethyl ether and water. The ether layer was separated, dried over magnesium sulfate and then concentrated under vacuum. The residue was purified by column chromatography (silica gel eluting with 10-20% ethyl acetate in hexanes v/v) to provide 1 g of 4-bis(phenylmethyl)amino-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-2-methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05482936
출처 데이터셋uspto-grants-1996_01
ORD IDord-db242ccd6c31490594b3cf4e65d94c64
출처 메모uspto-grants-1996_01