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HRID 21896作成日:2026年10月26日

Hydrochloric Acid → trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxy-N-benzenesulphonylcyclohexanecarboxamide

https://huagongshe.com/reaction/21896

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BenzenesulfonamideHCID 7370—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxycyclohexanecarboxylic acidHCID 15728507—
溶媒TetrahydrofuranHCID 8028—
生成物trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxy-N-benzenesulphonylcyclohexanecarboxamideHCID 152396336.7%

反応手順

trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxycyclohexanecarboxylic acid (1.0 g), prepared as in Example 11, in dry tetrahydrofuran (10 ml) was added dropwise to a stirred solution of 1,1-carbonyldiimidazole (0.57 g) in dry tetrahydrofuran (10 ml) under nitrogen. The reaction mixture was stirred 30 minutes at ambient temperature, heated to reflux for 30 minutes and cooled to ambient temperature. Benzenesulphonamide (0.56 g) was added followed by dropwise addition of 1,8-diazabicyclo (5.4.0) undec-7-ene (0.54) in dry tetrahydrofuran (5 ml). The reaction mixture was stirred for 24 hours at ambient temperature, refluxed for 6 hours then poured into 1N hydrochloric acid (80 ml) and extracted with 3×100 ml portions of diethyl ether. The combined ether extracts were dried over magnesium sulphate and evaporated. The residue was chromatographed on silica-gel, using a 2:1 dichloromethane/ethyl acetate eluant, to give 100 mg of the title compound, melting point 175° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426090
出典データセットuspto-grants-1995_06
ORD IDord-66998b7f00e74f96b7a19de6d7beba6e
出典メモuspto-grants-1995_06