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HRID 216760作成日:2026年10月23日

Hydrochloric Acid → 3-((9H-Purin-6-ylthio)methyl)-8-methyl-2-o-tolylquinoline

https://huagongshe.com/ja/reaction/216760

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Carbon tetrabromideHCID 11205—
反応物TriphenylphosphineHCID 11776—
反応物Sodium HydroxideHCID 14798—
反応物(8-Methyl-2-o-tolylquinolin-3-yl)methanolHCID 57707986—
反応物3-(Bromomethyl)-8-methyl-2-(2-methylphenyl)quinolineHCID 57708065—
反応物HCID 178527204HCID 178527204—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物3-((9H-Purin-6-ylthio)methyl)-8-methyl-2-o-tolylquinolineHCID 178424199—

反応条件

温度0 °C

反応手順

Solid carbontetrabromide (429 mg, 1.29 mmol) was added to a mixture of (8-methyl-2-o-tolylquinolin-3-yl)methanol (227 mg, 0.86 mmol) and triphenylphosphine (339 mg, 1.29 mmol) in CH2Cl2 (5 mL) at 0° C., and the mixture was stirred at 0° C. for 0.5 h. The crude mixture was concentrated under reduced pressure, evaporated onto silica gel, and purified by flash chromatography (Biotage® Si 25+M) eluting with EtOAc/hexane (0% to 10%) to provide an off-white solid; used without further purification, MS (ESI+) m/z=326.0 (M). A 2.0M aqueous solution of sodium hydroxide (0.86 mL, 1.72 mmol) was added to a mixture of 3-(bromomethyl)-8-methyl-2-o-tolylquinoline (140 mg, 0.43 mmol) and 6-mercaptopurine monohydrate (146 mg, 0.86 mmol) in THF (1.6 mL), and the biphasic mixture was heated under reflux for 5 h. The reaction mixture was cooled to 0° C., neutralized by the addition of 1N aqueous HCl, diluted with brine (10 mL), and extracted with THF (3×15 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. The resulting yellow solid was dissolved in THF/DMSO, evaporated onto silica gel, and purified by flash chromatography (Biotage® Si 25+M) eluting with acetone/hexane (20% to 50%). The resulting off-white solid was recrystallized from THF/MeOH to provide a white solid [PI3δ IC50=889 nM]. MS (ESI+) m/z=398.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193199B2
出典データセットuspto-grants-2012_06
ORD IDord-a7b224a9d4854de6867ce8a8e31ea2ee
出典メモuspto-grants-2012_06