Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1924866생성일: 2026년 10월 26일
3-Tert-butyl-1,2-oxazol-5-amine → N-(3-tert-Butyl-isoxazol-5-yl)-4-hydroxy-2-methyl-2-(tetrahydro-pyran-4-sulfonyl)-butyramide
https://huagongshe.com/reaction/1924866
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Tert-butyl-1,2-oxazol-5-amine | HCID 2095694 | — |
| 반응물 | Trimethylaluminum | HCID 16682925 | — |
| 반응물 | 3-Methyl-3-(tetrahydro-pyran-4-sulfonyl)-dihydro-furan-2-one | HCID 58280579 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(3-tert-Butyl-isoxazol-5-yl)-4-hydroxy-2-methyl-2-(tetrahydro-pyran-4-sulfonyl)-butyramide | HCID 44609910 | 69.3% |
반응 단계
To a solution of 3-tert-butyl-isoxazol-5-ylamine (0.421 g; 3.00 mmol) in methylene chloride (10 mL) was added dropwise the trimethylaluminum (1.50 mL of a 2.0 M solution in toluene; 3.0 mmol). The mixture was stirred 15 minutes and 3-methyl-3-(tetrahydro-pyran-4-sulfonyl)-dihydro-furan-2-one (0.596 g; 2.40 mmol) was added. The mixture was heated to 45° C. overnight, cooled to room temperature, carefully quenched with 0.5 mL methanol, applied to a plug of silica gel and eluted with ethyl acetate. Removal of the volatiles in vacuo provided a residue which was purified by silica gel chromatography using ethyl acetate and hexanes as the eluent. The product-rich fractions were concentrated in vacuo to provide 0.646 g of the desired product. 1H NMR (CDCl3) δ 9.92 (bs, 1H), 6.29 (s, 1H), 4.11-3.92 (m, 4H), 3.86 (m, 1H), 3.60 (m, 1H), 3.40 (m, 2H), 2.57 (m, 1H), 2.36 (m, 1H), 2.12-1.90 (m, 4H), 1.80 (s, 3H), 1.32 (s, 9H). MS (ESI): m/e 389 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08178568B2 |
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| 출처 데이터셋 | uspto-grants-2012_05 |
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| ORD ID | ord-81e0d7b338aa40ad89fe7838a514abee |
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| 출처 메모 | uspto-grants-2012_05 |
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