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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81532생성일: 2026년 10월 24일

[5-(3-Azido-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester → HCID 66665607, 화합물

https://huagongshe.com/ko/reaction/81532

반응식

참여 물질

역할이름HCID투입량
반응물[5-(3-Azido-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl esterHCID 86650252—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물HCID 66665607HCID 66665607—

반응 단계

A solution of 740 mg (2.118 mmol) [5-(3-azido-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester (Example 31h) in 5 ml THF and 5 ml EtOH was stirred in the presence of 35 mg 10% Pd—C under hydrogen. After 3 h the mixture was filtered over celite, concentrated and crystallized from EtOAc/hexane to give a beige solid. The racemic product was separated via prep HPLC on Chiralpak AD-H 250×4.6 mm column using heptan/EtOH 1:1 as an eluent. The desired compound was the slower eluting (R)-enantiomer. TLC: Rf (Hexane/EtOAc 2:1)=0.15. HPLC: RtH=1.764 min; ESIMS [M+H]+=324. 1H-NMR (CDCl3, 360 MHz, broad signals due to hindered rotation): 10.5 (br, 1H), 7.12 (br, 1H), 6.69 (d, 1H), 6.59 (br d, 1H), 4.8-4.0 (m, 8H), 1.48 (br s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846658B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9da3b1b7d6e046a3be9b62af4e12711d
출처 메모uspto-grants-2014_09