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HRID 2220096作成日:2026年10月26日

Methyl chloroformate → 4-(3-Methylsulfanyl-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/2220096

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl chloroformateHCID 6586—
反応物TriethylamineHCID 8471—
反応物1,2,3,6-Tetrahydro-4-(3-(methylthio)phenyl)pyridineHCID 12988965—
溶媒DichloromethaneHCID 6344—
生成物4-(3-Methylsulfanyl-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl esterHCID 12988966—

反応条件

温度0 °C

反応手順

4-(3-Methylsulfanyl-phenyl)-1,2,3,6-tetrahydropyridine (2 g) and NEt3 (1 g) were dissolved in CH2Cl2 (75 ml) and cooled to 0° C. Methyl chloroformate (0.96 g) dissolved in CH2Cl2 (20 ml) was added dropwise and the reaction mixture was then allowed to reach room temperature. After an additional two hours at room temperature the reaction mixture was washed with 10% Na2CO3 solution, dried (MgSO4), filtered and concentrated by evaporation. The oily residue was chromatographed on a silica column using CH2Cl2:MeOH (19:1 (v/v)) as eluent, 4-(3-methylsulfanyl-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester (1.4 g). MS m/z (relative intensity, 70 eV) 263 (M+45), 248 (89), 129 (83), 128 (bp), 59 (96).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07417043B2
出典データセットuspto-grants-2008_08
ORD IDord-4c194305f90046309ed081fb8fb6c1aa
出典メモuspto-grants-2008_08