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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

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물QuinolineHCID 7047—
반응물TriethylamineHCID 8471—
반응물(+)-PantolactoneHCID 736053—
반응물(3S)-3-amino-2-hydroxy-N-[(1R)-1-phenylethyl]heptanamideHCID 11265560—
용매TetrahydrofuranHCID 8028—
생성물(3s)-4,4-dimethyl-2-oxotetrahydro-3-furanyl (1S)-1-(1-hydroxy-2-oxo-2-{[(1r)-1-phenylethyl]amino}ethyl)pentylcarbamateHCID 9113560385.1%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402606B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-827e5a6be30e4be79a7221af68c7c399
출처 메모uspto-grants-2008_07