Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1094341생성일: 2026년 10월 26일
Sodium borohydride → (S)-N-(3,4-Dimethyl-phenyl)-2-(4-fluoro-phenyl)-2-hydroxy-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamide
https://huagongshe.com/reaction/1094341
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | N-(3,4-Dimethyl-phenyl)-2-(4-fluoro-phenyl)-2-oxo-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamide | HCID 58007489 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (S)-N-(3,4-Dimethyl-phenyl)-2-(4-fluoro-phenyl)-2-hydroxy-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamide | HCID 44546250 | 97% |
반응 단계
A solution of N-(3,4-dimethyl-phenyl)-2-(4-fluoro-phenyl)-2-oxo-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamide (515 mg, 1.16 mmol) was dissolved in MeOH (8 mL), cooled to 0° C. and treated with NaBH4 (88 mg, 2.33 mmol) and stirred for 12 h at ambient temperature. The reaction mixture was quenched with aqueous K2CO3 (2 M, 1 mL), concentrated, then redissolved in EtOAc (15 mL) and washed with aqueous K2CO3 (2 M, 3×15 mL). The combined aqueous layers were extracted with EtOAc (3×15 mL) and the combined organic layers dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=95:5 to 60:40) afforded the racemic compound (501 mg, 97%) as a lightyellow oil. Separation by chromatography on a chiral column provided the title compound as a colourless oil MS m/e: 447.2 [M+H]+ which crystallized upon standing.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08133909B2 |
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| 출처 데이터셋 | uspto-grants-2012_03 |
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| ORD ID | ord-666807874528473fb23a749e7ef89065 |
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| 출처 메모 | uspto-grants-2012_03 |
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