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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1704516생성일: 2026년 10월 24일

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/ko/reaction/1704516

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium CarbonateHCID 10340—
반응물5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 104607—
반응물3-(3-bromopropyl)-2(3H)-benzothiazoloneHCID 21459927—
용매WaterHCID 962—
용매Methyl Isobutyl KetoneHCID 7909—
생성물5-chloro-1,3-dihydro-1-{1-[3-(2-oxo-3(2H)-benzothiazolyl)propyl]-4-piperidinyl}-2H-benzimidazol-2-oneHCID 2038557231%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04126687
출처 데이터셋uspto-grants-1978_11
ORD IDord-a87d90f063924e649db597b7104f86ee
출처 메모uspto-grants-1978_11