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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1473410생성일: 2026년 10월 26일

Benzyl mercaptan → 7-(Benzylthio)-4-chloroquinoline

https://huagongshe.com/reaction/1473410

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl mercaptanHCID 7509—
반응물1,4-DioxaneHCID 31275—
반응물DiisopropylethylamineHCID 81531—
반응물7-Bromo-4-ChloroquinolineHCID 10800239—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
생성물7-(Benzylthio)-4-chloroquinolineHCID 8668745789%

반응 단계

A 250-mL 3-neck round-bottom flask was charged with 7-bromo-4-chloroquinoline (BioBlocks, Inc., San Diego, Calif.; 7.000 g, 28.9 mmol), Xantphos (0.835 g, 1.443 mmol), and Pd2(dba)3 (0.661 g, 0.722 mmol), and after flushing with argon, dioxane (57.7 ml) and n,n-diisopropylethylamine (10.08 ml, 57.7 mmol) were added in sequence. The flask was fitted with a reflux condenser, and was placed in a heating bath at 80° C. for 10 minutes, after which benzyl mercaptan (3.58 ml, 30.3 mmol) was added drop wise via syringe. The reaction was stirred for 20 minutes until completion. The material was diluted with water, and washed with DCM (×3), and the combined organics were dried via phase separator (Radley's Technology) and concentrated under a vacuum. Upon dissolving the material in DCM, solids remained out of solution, and they were filtered off and washed with DCM. The corresponding filtrate was concentrated under a vacuum and purified via silica gel chromatography (120-g column) eluting with 0 to 100% ethyl acetate in heptanes to yield 7-(benzylthio)-4-chloroquinoline (7.35 g, 25.7 mmol, 89% yield) as a light yellow solid. m/z (ESI) 286.0 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012443B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-ea8141a6744f44db846ca66751ba2da8
출처 메모uspto-grants-2015_04