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HRID 2892作成日:2026年10月25日

Guanidine → N-diaminomethylene-2-methyl-4-(1-cyclopenten-3-yl)-5-methylsulfonylbenzamide

https://huagongshe.com/reaction/2892

反応式

関与物質

役割名称HCID仕込み量
反応物GuanidineHCID 3520—
反応物CyclopenteneHCID 8882—
反応物SodiumHCID 5360545—
反応物Carbamimidoylazanium ChlorideHCID 5460839—
反応物2-Methyl-4-(1-cyclopentene-3-yl)-5-methylsulfonylbenzoyl chlorideHCID 15338768—
反応物Methyl 2-methyl-4-bromo-5-methyl-sulfonyl-benzoateHCID 86752332—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物N-diaminomethylene-2-methyl-4-(1-cyclopenten-3-yl)-5-methylsulfonylbenzamideHCID 9818569—

反応手順

A fresh guanidine solution prepared from 5.6 g of guanidinium chloride and 1.6 g of sodium in 40 ml of ethylene glycol dimethyl ether is added to a solution of 1.2 g of 2-methyl-4-(1-cyclopentene-3-yl)-5-methylsulfonylbenzoyl chloride [obtainable by reaction of methyl 2-methyl-4-bromo-5-methyl-sulfonyl-benzoate with cyclopentene in the presence of Pd(II)acetate and tri-o-tolylphosphine, separation of the two isomers by means of a Prebar® stainless steel cartridge 250-50, filled with LiChroprep RP-18; eluent 0.1 m NaH2PO4 buffer/acetonitrile 9:1 with an increasing gradient to 1:1, and subsequent hydrolysis and conversion into the acid chloride with SOCl2 ], in 20 ml of ethylene glycol dimethyl ether with ice-cooling and the mixture is stirred at room temperature for 2 hours. The reaction mixture is then poured onto ice-water, acidified and washed with ethyl acetate and the pH of the solution is adjusted to 10. Customary working-up gives N-diaminomethylene-2-methyl-4-(1-cyclopentene-3-yl)-5-methylsulfonylbenzamide, which can be recrystallized from acetonitrile/diethyl ether, melting point 212°-214°.

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-f0a8b290beed4251bf550b18be2b89c0
出典メモuspto-grants-1998_03