Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | D-tert-leucine | HCID 6950340 | — |
| 반응물 | 8-methyl-2-(4-methyl-phenyl)-1,5-benzothiazepine-3,4(2H,5H)-dione | HCID 19026137 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one | HCID 10566075 | 93.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05310904 |
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| 출처 데이터셋 | uspto-grants-1994_05 |
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| ORD ID | ord-3ef924ee835c48d98f8dd4a0dc73ee24 |
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| 출처 메모 | uspto-grants-1994_05 |
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