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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072259생성일: 2026년 10월 26일

Cetirizine → Cetirizine Hydrochloride

https://huagongshe.com/reaction/1072259

반응식

참여 물질

역할이름HCID투입량
반응물CetirizineHCID 2678—
반응물4-((4-Chlorophenyl)phenylmethyl)-1-piperazineethanolHCID 3419898—
반응물PotassiumHCID 5462222—
반응물Potassium tert-butoxideHCID 23665647—
반응물Sodium chloroacetateHCID 23665759—
생성물Cetirizine HydrochlorideHCID 5518248.8%

반응 단계

The process of UK-P No. 2 225 320 (Chem. Abstr., 113, 191395s) aims at the elimination of the disadvantages of the above known processes by preparing cetirizine from the {2-[4-(α-phenyl-p-chlorobenzyl)piperazin-1-yl]}ethanol of the formula III which is converted to the potassium salt with potassium tert-butylate. The potassium salt is reacted with sodium chloro-acetate to obtain cetirizine dihydrochloride in a yield of 48.8%. In addition, 5.1% of a second generation product are obtained. Also an improved process is described for the preparation of the {2-[4-(α-phenyl-p-chlorobenzyl)piperazin-1-yl]}ethanol of the formula III according to which 1-[(4-chlorophenyl)phenyl-methyl]piperazine of the formula VI is reacted with ethylene chlorohydrine in a yield of 90.4%, the total yield of the synthesis, referred to the piperazine derivative of the formula VI, is merely 48.7%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06908999B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-a63f0f0fe1ef487fa2253d6c3dd5f958
출처 메모uspto-grants-2005_06