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HRID 1580464作成日:2026年10月27日

Ammonia → Cyclopentylurea

https://huagongshe.com/reaction/1580464

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物CyclopentylamineHCID 2906—
反応物Cyclooctanone semicarbazoneHCID 3348066—
溶媒1,4-DioxaneHCID 31275—
生成物CyclopentylureaHCID 294526—

反応手順

1.8 g of 4-[4-(β-<2-methoxy-5-chloro-benzamido>-ethyl)-benzenesulfonyl]-cyclooctanone-semicarbazone, 50 ml of dioxane and 0.29 g of cyclopentyl-amine were refluxed for 1 hour. The clear solution was concentrated in vacuo and the residue obtained was treated with about 0.5 %-aqueous ammonia. After filtration the filtrate was acidified. A crystalline precipitate of N-[4-(β-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl]-N'-cyclopentyl-urea was obtained, separated by suction-filtration, dried and recrystallized from methanol. The melting point of the substance was 182° - 184°C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03932658
出典データセットuspto-grants-1976_01
ORD IDord-89c5288613194b2bb0053f6c99037581
出典メモuspto-grants-1976_01