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HRID 1033477생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium borohydrideHCID 4311764—
반응물D-tert-leucineHCID 6950340—
반응물8-methyl-2-(4-methyl-phenyl)-1,5-benzothiazepine-3,4(2H,5H)-dioneHCID 19026137—
용매TetrahydrofuranHCID 8028—
생성물(2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-oneHCID 1056607593.6%

반응 조건

온도-10 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05310904
출처 데이터셋uspto-grants-1994_05
ORD IDord-3ef924ee835c48d98f8dd4a0dc73ee24
출처 메모uspto-grants-1994_05