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HRID 1033477作成日:2026年10月27日

Acetic Acid → (2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one

https://huagongshe.com/reaction/1033477

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium borohydrideHCID 4311764—
反応物D-tert-leucineHCID 6950340—
反応物8-methyl-2-(4-methyl-phenyl)-1,5-benzothiazepine-3,4(2H,5H)-dioneHCID 19026137—
溶媒TetrahydrofuranHCID 8028—
生成物(2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-oneHCID 1056607593.6%

反応条件

温度-10 °C

反応手順

A mixture of D-tert-leucine (289 mg), sodium borohydride (76 mg) and tetrahydrofuran (15 ml) is refluxed under nitrogen atmosphere for three hours. The mixture is cooled to -10° C., and thereto is added a solution of 8-methyl-2-(4-methyl-phenyl)-1,5-benzothiazepine-3,4(2H,5H)-dione (297 mg) in tetrahydrofuran (3 ml). The mixture is stirred at -10° C. for 17 hours, and thereto is added acetic acid (600 mg). The mixture is evaporated under reduced pressure to remove the solvent. To the residue is added water (10 ml), and the precipitated crystal is collected by filtration, washed with water, and dried to give (2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one (280 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05310904
出典データセットuspto-grants-1994_05
ORD IDord-3ef924ee835c48d98f8dd4a0dc73ee24
出典メモuspto-grants-1994_05