Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 750378생성일: 2026년 10월 26일
Phosgene → (3s)-4,4-dimethyl-2-oxotetrahydro-3-furanyl (1S)-1-(1-hydroxy-2-oxo-2-{[(1r)-1-phenylethyl]amino}ethyl)pentylcarbamate
https://huagongshe.com/reaction/750378
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | Quinoline | HCID 7047 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (+)-Pantolactone | HCID 736053 | — |
| 반응물 | (3S)-3-amino-2-hydroxy-N-[(1R)-1-phenylethyl]heptanamide | HCID 11265560 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (3s)-4,4-dimethyl-2-oxotetrahydro-3-furanyl (1S)-1-(1-hydroxy-2-oxo-2-{[(1r)-1-phenylethyl]amino}ethyl)pentylcarbamate | HCID 91135603 | 85.1% |
반응 단계
Phosgene (1.04 mL, 1.93 M, 2.00 mmol) was added dropwise to a solution of (S)-(+)-pantolactone (130 mg, 1.00 mmol) and quinoline (0.241 mL, 2.00 mmol) in anhydrous tetrahydrofuran (3 mL) at 0° C. under nitrogen. The cold bath was removed, and the mixture was stirred for 18 h at room temperature. Volatiles were then removed under vacuum, and the resulting solid was slurried in anhydrous tetrahydrofuran (4 mL) under nitrogen. A solution of triethylamine (0.153 mL, 1.10 mmol) and (3S)-3-amino-2-hydroxy-N-[(1R)-1-phenylethyl]heptanamide (264 mg, 1.00 mmol) in anhydrous tetrahydrofuran was added. The resulting mixture was stirred for 18 h, and was then partitioned between ethyl acetate (70 mL) and 1 N hydrochloric acid (35 mL). The ethyl acetate layer was washed further with two 35 mL portions of 1 N hydrochloric acid, followed by saturated aqueous sodium chloride (35 mL). After drying over magnesium sulfate, volatiles were removed to afford (3S)-4,4-dimethyl-2-oxotetrahydro-3-furanyl (1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)pentylcarbamate as a tan oil (358 mg, 85%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07402606B2 |
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| 출처 데이터셋 | uspto-grants-2008_07 |
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| ORD ID | ord-827e5a6be30e4be79a7221af68c7c399 |
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| 출처 메모 | uspto-grants-2008_07 |
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