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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10969생성일: 2026년 10월 24일

Acetic Acid → (6S,8R)-allyl-(8-azido-8-methyl-4-oxo-6-phenylcarbamoyl-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidin-3-yl)-carbamic Acid Benzyl Ester

https://huagongshe.com/ko/reaction/10969

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2,4,6-Triisopropylbenzenesulfonyl azideHCID 371707—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물(6S,8RS)-allyl-(8-methyl-4-oxo-6-phenylcarbamoyl-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidin-3-yl)-carbamic Acid Benzyl EsterHCID 69600916—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(6S,8R)-allyl-(8-azido-8-methyl-4-oxo-6-phenylcarbamoyl-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidin-3-yl)-carbamic Acid Benzyl EsterHCID 8659067165%

반응 조건

온도-78 °C

반응 단계

To a solution of the methyl diastereomers (18c) (3.90 g, 8.51 mmol) in 40 mL THF at −78° C., was added LiHMDS (IM in THF, 17.9 mL, 17.9 mmol). The red solution was stirred at −78° C. for 5 min, then a solution of trisyl azide (2.90 g, 9.36 mmol) in 8 mL THF was added. The reaction was stirred at −78° C. for 1.5 h, then was quenched with the addition of AcOH (2.19 mL, 38.3 mmol). The mixture was stirred at rt for 1 h, then was diluted with EtOAc. The organic phase was washed with 1N HCl, H2O and brine, dried (Na2SO4), and concentrated. The product was purified by flash chromatography (35 to 40% EtOAc/hexanes) to afford 2.764 g (65%) of azide 18d. MS (ESI) 500.4 (M+H+), 522.4 (M+Na+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094783B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-832d2b39b7bf4896951ab0ab2b27acfd
출처 메모uspto-grants-2006_08