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HRID 1666924作成日:2026年10月25日

(5R)-3-Isopropyl-5-phenyl-5,6-dihydro-2H-1,4-oxazin-2-one → (3S,5R)-3-Isopropyl-5-phenyl-3,4,5,6-tetrahydro-2H-1,4-oxazin-2-one

https://huagongshe.com/reaction/1666924

反応式

関与物質

役割名称HCID仕込み量
反応物(5R)-3-Isopropyl-5-phenyl-5,6-dihydro-2H-1,4-oxazin-2-oneHCID 59843746—
触媒Adams' catalystHCID 345198—
溶媒DichloromethaneHCID 6344—
生成物(3S,5R)-3-Isopropyl-5-phenyl-3,4,5,6-tetrahydro-2H-1,4-oxazin-2-oneHCID 12413874—

反応手順

To a solution of (5R)-3-isopropyl-5-phenyl-5,6-dihydro-2H-1,4-oxazin-2-one (38) (1.03 g, 4.74 mmol, 1.0 equiv.) in anhydrous dichloromethane (50 mL) under an atmosphere of nitrogen was added PtO2 (103 mg, 0.1 equiv.). The mixture was consecutively degassed and purged three times with hydrogen and then stirred for 5 hours under an atmosphere of hydrogen. Filtration through a short pad of CELITE® diatomaceous earth and removal of solvent from the filtrate in vacuo yielded the crude product which was purified by flash column chromatography on silica eluting with petrol and diethyl ether (4:1) to furnish the title product as a waxy solid (662 mg, 64%); m.p. 61.5-62.5° C.; v(max)(KBr) 3326 (N—H—), 2960 (C—H), 1733 (C═O), cm−1; δH (250 MHz, CDCl3) 7.47-7.35 (5H, m, Ph); 4.33-4.18 (3H, m, PhCHCH2), 3.81 (1H, m, NHCH), 2.49, (1H, m, CH(CH3)2), 1.68 (1H, br, NH), 1.09 (3H, dd, J 6.75 Hz, CH(CH3)2×3), 1.05 (3H, dd, J 6.75, CH(CH3)2×3); δC, (62.5 MHz, CDCl3) 170.3, 138.5, 129.3, 129.1, 127.6, 74.9, 64.2, 57.3, 32.0, 19.4, 17.4; m/z (Cl, NH3), 237 (MNH4+, 5%), 220 (100%, MH+), 219 (22%), and 216 (6%); HRMS for C13H18NO2 requires 220.1333 found 220.1338. [α]D20 −92.1 (c 1.45 CHCl3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044173B2
出典データセットuspto-grants-2011_10
ORD IDord-26ef0436d3b046d7ab3673110a22d61a
出典メモuspto-grants-2011_10