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HRID 900063作成日:2026年10月27日

Isobutyl Acetate → Mycophenolate Mofetil

https://huagongshe.com/reaction/900063

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutyl AcetateHCID 8038—
反応物2-MorpholinoethanolHCID 61163—
反応物Stannous chloride dihydrateHCID 61436—
反応物Mycophenolic AcidHCID 446541—
生成物Mycophenolate MofetilHCID 5281078—

反応手順

A mixture of mycophenolic acid (192 g, 0.6 mol) and 4-(2-hydroxyethyl)-morpholine (440 ml, 6 molar equivalents) was stirred at 150-155° C. for 4 hours in the presence of tin(II) chloride dihydrate (20.4 g, 0.15 molar equivalents) under nitrogen atmosphere. After the completion of the reaction, the reaction mixture was allowed to cool to room temperature. The obtained dark liquid was poured into isobutyl acetate (4.0 l). The solution was extracted with 2% of aqueous sodium bicarbonate solution (1.2 l, then 2×0.4 l). After the first addition of sodium bicarbonate solution the formed two-phase system was treated with charcoal (40 g) and filtrated (an emulsion was filtered off). The solution was extracted with water (1 l). -After phase separation the organic phase was washed with water (1 l) and evaporated to dryness at 40-50° C. under vacuum. To the solid material acetone (400 ml) and isopropanol (3.8 l) were added and the mixture was warmed to 40-45° C. (the material was dissolved). The solution was cooled to −5° C. during 6 hours and it was stirred at this temperature for 10-12 hours. After filtration, the crystals were washed with 2:19 acetone/isopropanol mixture (420 ml). The crude compound was dried in vacuum at 60° C. The yield was 169-195 g (65-75%). HPLC impurity profile: MPA=0.1%. Assay: 99.85%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07358247B2
出典データセットuspto-grants-2008_04
ORD IDord-7dd091eca18d4124b5ee7bd8e76176fb
出典メモuspto-grants-2008_04