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HRID 478052作成日:2026年10月26日

Methanesulfonic Acid → Tilomisole

https://huagongshe.com/reaction/478052

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物3-(p-Chlorophenyl)-2,3,-dihydro-3-hydroxythiazolo[3,2-a]benzimidazol-2-acetic acid, hydrobromideHCID 12281806—
反応物Acetate acetic acidHCID 21252148—
反応物Ethyl acetate acetateHCID 22609514—
溶媒WaterHCID 962—
生成物TilomisoleHCID 4274796.6%

反応手順

A mixture of 100 g of 3-(p-Chlorophenyl)-2,3,-dihydro-3-hydroxythiazolo[3,2-a]benzimidazol-2-acetic acid, hydrobromide and 200 ml of methanesulfonic acid was stirred overnight in a 500 ml round bottom flask. Thin layer chromatography on silica plates (solvent ethyl acetate/acetic acid) indicated rapid formation of an intermediate. After 20 hours at room temperature thin layer chromatography (silica plates, ethyl) acetate/acetic acid) showed the presence of a single component. The mixture was poured into water and the resulting crystals removed by filtration. The crystalline product was suspended in 5 volumes of hot water for 1/2 hour, filtered and the procedure repeated. After a final aqueous wash the material was dried in vacuo to yield the title compound (75 g, 91%) m.p. 242°-3° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04889936
出典データセットuspto-grants-1989_12
ORD IDord-38716f1ad7844c2bb4923765ba2ae21d
出典メモuspto-grants-1989_12