(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

HRID 1666924Notes

Reaction equation

HRID 1666924 reaction equation
[CH:1]([C:4]1[C:5](=[O:16])[O:6][CH2:7][C@@H:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[N:9]=1)([CH3:3])[CH3:2]>ClCCl.O=[Pt]=O>[CH:1]([C@@H:4]1[NH:9][C@H:8]([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:7][O:6][C:5]1=[O:16])([CH3:3])[CH3:2]

Participants

4

Procedure

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).

Workup

  1. customThe mixture was consecutively degassed
  2. custompurged three times with hydrogen
  3. filtrationFiltration
  4. customthrough a short pad of CELITE® diatomaceous earth and removal of solvent from the filtrate in vacuo
  5. customyielded the crude product which
  6. customwas purified by flash column chromatography on silica eluting with petrol and diethyl ether (4:1)

Sources & evidence

ORD record
ord-26ef0436d3b046d7ab3673110a22d61a
Source dataset
uspto-grants-2011_10
Patent number
US08044173B2

Reaction notes

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