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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 926586생성일: 2026년 10월 26일

Sodium Chloride → (4-Chloro-2-methoxy-3-(4-methylbenzyl)quinolin-6-yl)(2,6-dimethylpyridin-3-yl)(1-methyl-1H-1,2,3-triazol-5-yl)methanol

https://huagongshe.com/reaction/926586

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물(2,6-Dimethylpyridin-3-yl)(1-methyl-1H-1,2,3-triazol-5-yl)methanoneHCID 86715642—
반응물4-Chloro-6-iodo-2-methoxy-3-(4-methylbenzyl)quinolineHCID 118006249—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(4-Chloro-2-methoxy-3-(4-methylbenzyl)quinolin-6-yl)(2,6-dimethylpyridin-3-yl)(1-methyl-1H-1,2,3-triazol-5-yl)methanolHCID 118006555—

반응 단계

A solution of n-butyllithium in hexanes (2.5 M, 0.47 mL, 1.2 mmol) was added dropwise to a stirring solution of 4-chloro-6-iodo-2-methoxy-3-(4-methylbenzyl)quinoline (500 mg, 1.2 mmol, Intermediate 22: step c) in tetrahydrofuran (9 mL) at −78° C. After 2 minutes, a solution of (2,6-dimethylpyridin-3-yl)(1-methyl-1H-1,2,3-triazol-5-yl)methanone (255 mg, 1.2 mmol, Intermediate 19: step b) in tetrahydrofuran (2 mL) was added dropwise. After 5 minutes, the flask was placed into an ice-water bath. After 15 minutes, water (5 mL) and ethyl acetate (50 mL) were added and the biphasic mixture was poured into saturated aqueous sodium chloride solution (15 mL). The layers were separated. The organic layer was dried with sodium sulfate and the dried solution was filtered. Silica gel (6 g) was added to the filtrate and the mixture was concentrated by rotary evaporation to afford a free-flowing powder. The powder was loaded onto a silica gel column for flash column chromatography purification. Elution with 100% hexanes initially, grading to 100% ethyl acetate provided the title compound as a white foam. MS (ESI): mass calcd. for C29H28ClN5O2, 513.2. m/z found, 514.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09284308B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-354b2189a2ba46c38d1de97039a17ee7
출처 메모uspto-grants-2016_03