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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1610046생성일: 2026년 10월 24일

Atenolol → Esatenolol

https://huagongshe.com/ko/reaction/1610046

반응식

참여 물질

역할이름HCID투입량
반응물AtenololHCID 2249—
반응물IsopropylamineHCID 6363—
반응물Diglycidyl etherHCID 16704—
생성물EsatenololHCID 175540—

반응 단계

In order to prevent the reaction of produced atenolol with the optically active glycidyl ether (4) it is preferable to add the optically active glycidyl ether (4) to isopropyl amine in a solvent. The removal of excess isopropyl amine by distillation gave desired (S)-atenolol (1). Preferably, the distillation is carried out at atmospheric pressure at the initial stages and under reduced pressure at later stages, keeping the reaction mass temperature below 60° to 70° C., through out the distillation process. The crude residue may be purified, if required, by dissolving it in 1N HCl, treating this solution with activated charcoal, filtering the charcoal followed by treatment of alkali to precipitate the product. Thus, the solid product was isolated by conventional method such as filtration to get (S)-atenolol (1) of optical purity of 98% ee and above. If, necessary, the optically active (S)-atenolol (1) may be crystallized from an appropriate solvent such as water, alcohols, such as methanol, ethanol, isopropyl alcohol, butanol etc., ethers, such as diethyl ether, methyl tbutyl ether, diisopropyl ether or ketones, such as acetone, ethyl methyl ketone, methyl isobutyl ketone etc.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06982349B1
출처 데이터셋uspto-grants-2006_01
ORD IDord-e2324558f6104b96bacdaf691ac0074a
출처 메모uspto-grants-2006_01