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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1383791생성일: 2026년 10월 26일

Salbutamol → Salbutamol glycodeoxycholate

https://huagongshe.com/reaction/1383791

반응식

참여 물질

역할이름HCID투입량
반응물SalbutamolHCID 2083—
반응물Ethyl AcetateHCID 8857—
반응물Glycodeoxycholic AcidHCID 3035026—
용매EthanolHCID 702—
생성물Salbutamol glycodeoxycholateHCID 131722754105.9%

반응 단계

Salbutamol base (1.2007 g; 5.02 mmol) was dissolved in ethanol (100 mL) with vigorous stirring. Glycodeoxycholic acid (2.4601 g; water content: 4.25% w/w; 5.25 mmol˜5% molar excess) was added and dissolved with stirring. A clear, colourless solution was obtained. The ethanol was removed by vacuum rotary-evaporation to give a viscous, yellow residue. Ethyl acetate (200 mL) was added to the residue and the mixture heated in a water bath with constant agitation. As the yellow residue dissolved, a white precipitate formed. Agitation was continued until the yellow residue disappeared. The ethyl acetate solution was cooled in an ice bath. The precipitate was isolated by vacuum filtration and dried in a vacuum oven at 40° C. for 20 hours to give salbutamol glycodeoxycholate (3.662 g; water content; 4.95% w/w; % yield; 97.9%). Analysis by differential scanning calorimetry from 50 to 200° C. gave no significant thermal event. Slow decomposition was evident after 110° C. A saturated aqueous solution gave a pH of 6.12. The aqueous solubility was greater than 8.35 mg/mL. The theoretical percentage of salbutamol base in the salbutamol glycodeoxycholate 34.74%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06255502B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-2df3eac4f00b4382adc03e49033db230
출처 메모uspto-grants-2001_07