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HRID 1383791作成日:2026年10月27日

Salbutamol → Salbutamol glycodeoxycholate

https://huagongshe.com/reaction/1383791

反応式

関与物質

役割名称HCID仕込み量
反応物SalbutamolHCID 2083—
反応物Ethyl AcetateHCID 8857—
反応物Glycodeoxycholic AcidHCID 3035026—
溶媒EthanolHCID 702—
生成物Salbutamol glycodeoxycholateHCID 131722754105.9%

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06255502B1
出典データセットuspto-grants-2001_07
ORD IDord-2df3eac4f00b4382adc03e49033db230
出典メモuspto-grants-2001_07