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HRID 971789作成日:2026年10月25日

Potassium Iodide → 5-chloro-1,3-dihydro-1-{1-[3-(2-oxo-3(2H)-benzothiazolyl)propyl]-4-piperidinyl}-2H-benzimidazol-2-one

https://huagongshe.com/reaction/971789

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Sodium CarbonateHCID 10340—
反応物5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 104607—
反応物3-(3-bromopropyl)-2(3H)-benzothiazoloneHCID 21459927—
溶媒WaterHCID 962—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物5-chloro-1,3-dihydro-1-{1-[3-(2-oxo-3(2H)-benzothiazolyl)propyl]-4-piperidinyl}-2H-benzimidazol-2-oneHCID 2038557231%

反応手順

A mixture of 5.4 parts of 3-(3-bromopropyl)-2(3H)-benzothiazolone, 4.5 parts of 5-chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one, 5.3 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 3 hours with water-separator. After cooling, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from a mixture of 4-methyl-2-pentanone and 2-propanone. The product is filtered off and dried, yielding 2.5 parts (31%) of 5-chloro-1,3-dihydro-1-{1-[3-(2-oxo-3(2H)-benzothiazolyl)propyl]-4-piperidinyl}-2H-benzimidazol-2-one; mp. 184.1° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04160836
出典データセットuspto-grants-1979_07
ORD IDord-be071f816a3b49fa8272f36598bcebb9
出典メモuspto-grants-1979_07