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HRID 2895作成日:2026年10月23日

Guanidine → N-diaminomethylene-2-methyl-4-ethenyl-5-methylsulfonyl-benzamide

https://huagongshe.com/ja/reaction/2895

反応式

関与物質

役割名称HCID仕込み量
反応物GuanidineHCID 3520—
反応物Methyl 4-bromo-5-methanesulfonyl-2-methylbenzoateHCID 10590825—
反応物N-diaminomethylene-2-methyl-4-ethynyl-5-methylsulfonylbenzamideHCID 19688115—
反応物Methyl 2-methyl-4-ethynyl-5-methylsulfonyl-benzoateHCID 19688249—
反応物HCID 178418361HCID 178418361—
触媒Calcium Palladium CarbonateHCID 12000666—
溶媒DimethylformamideHCID 6228—
生成物N-diaminomethylene-2-methyl-4-ethenyl-5-methylsulfonyl-benzamideHCID 19688146—

反応手順

6.0 g of N-diaminomethylene-2-methyl-4-ethynyl-5-methylsulfonylbenzamide, m.p. 223°-226° [obtainable by reaction of methyl 2-methyl-4-bromo-5-methylsulfonyl-benzoate with Li acetylide to give methyl 2-methyl-4-ethynyl-5-methylsulfonyl-benzoate and subsequent reaction with guanidine] are dissolved in 300 ml of DMF and hydrogenated in the presence of 450 mg of Pd-CaCO3 (Lindlar catalyst) for 15 minutes in a stream of hydrogen (p=1 bar). Customary working up gives N-diaminomethylene-2-methyl-4-ethenyl-5-methylsulfonyl-benzamide).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731351
出典データセットuspto-grants-1998_03
ORD IDord-b9a7eb44685f468d8f6ff10d7448f0ce
出典メモuspto-grants-1998_03