Oxygen → HCID 88377828, compound

HRID 1379962Notes

Reaction equation

[CH2:1]([N:8]([CH3:34])[C:9](=[O:33])[C@@H:10]([N:22]([CH2:30][CH:31]=C)[C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[CH2:11][C:12]1[CH:21]=[CH:20][C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=1)C1C=CC=CC=1.N1C=[CH:39][CH:38]=[CH:37][CH:36]=1.[O:41]=O.CSC.C(O[CH2:50][CH3:51])(=O)C>ClCCl.CO>[CH2:1]([N:8]([CH3:34])[C:9](=[O:33])[C@@H:10]([N:22]([CH2:30][CH:31]=[O:41])[C:23]([O:25][C:26]([CH3:28])([CH3:27])[CH3:29])=[O:24])[CH2:11][C:12]1[CH:21]=[CH:20][C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=1)[C:51]1[CH:50]=[CH:39][CH:38]=[CH:37][CH:36]=1

Participants

Conditions

Temperature: -78 °C

Procedure

Combine (S)-N-benzyl-N-methyl-2-[N'-(t-butoxycarbonyl)-allylamino]-3-(naphth-2-yl)-propionamide (3.34 g, 7.29 mmol), and pyridine (0.03 ml) in dichloromethane/methanol (66 mL/7 mL). Cool to -78° C. Pass ozonized oxygen through the solution until a persistent light blue color is obtained. Pass nitrogen through the solution until the blue color dissipates. Add dimethyl sulfide (12 mL). Allow the reaction mixture to warm to ambient temperature and stir for 16 hours. Concentrate in vacuo to obtain a residue. Dilute the residue with ethyl acetate and extract with water. Separate the layers, dry the organic layer over MgSO4, filter, and evaporate in vacuo. Chromatograph on silica gel eluting with 20% ethyl acetate/hexane to give the title compound: TLC Rf =0.70 (silica gel, 50% ethyl acetate/hexane).

Workup

customis obtained
temperatureto warm to ambient temperature
concentrationConcentrate in vacuo
customto obtain a residue
extractionextract with water
customSeparate the layers
dry with materialdry the organic layer over MgSO4
filtrationfilter
customevaporate in vacuo

Sources & evidence

ORD record: ord-9302b1cc728c4e99ae7bef7240eafea5
Source dataset: uspto-grants-1997_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05672602

Reaction notes

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