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HRID 221681作成日:2026年10月25日

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

https://huagongshe.com/reaction/221681

反応式

関与物質

役割名称HCID仕込み量
反応物[5-(3-Azido-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl esterHCID 86650252—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 66665607HCID 66665607—

反応手順

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: RtH4=1.764 min; ESIMS [M+H]+=324.11 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207164B2
出典データセットuspto-grants-2012_06
ORD IDord-f7df5f9fb0d046539a2b94723c680f9e
出典メモuspto-grants-2012_06