Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73020생성일: 2026년 10월 25일
(2-Oxopropyl)amine → N-acetonyl-8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxamide
https://huagongshe.com/reaction/73020
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (2-Oxopropyl)amine | HCID 215 | — |
| 반응물 | 2-Methyltetrahydrofuran | HCID 7301 | — |
| 반응물 | Propylphosphonic anhydride | HCID 111923 | — |
| 반응물 | 8-Benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxylic acid | HCID 70872865 | — |
| 생성물 | N-acetonyl-8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxamide | HCID 70872809 | 41% |
반응 단계
To 8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxylic acid (201 mg, 0.43 mmol), 1-aminopropan-2-one (47 mg, 0.43 mmol) and T3P (641 μL of 50% w/w, 1.08 mmol) was added 2-methyltetrahydrofuran (1 mL) and the reaction mixture was then heated at 75° C. for 2 hours. The reaction mixture was cooled to room temperature and partitioned between EtOAc/saturated aq. NaHCO3. The layers were separated and the aqueous layer was extracted with EtOAc (2×). The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to a dark foam. The crude product was purified by silica gel column chromatography using 20-70% EtOAC in DCM as eluent to afford N-acetonyl-8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxamide (92 mg, 41%) as a yellow solid. ESI-MS m/z calc. 521.6. Found 522.5 (M+1)+; Retention time: 1.48 minutes (3 min run).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08828996B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-a63a11ff627644b2bd4a434656b948bd |
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| 출처 메모 | uspto-grants-2014_09 |
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