HCID 15228020, compound → HCID 54064094, compound

HRID 864259Notes

Reaction equation

HRID 864259 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:13][C@H:12]([CH2:14][N:15]3[CH2:20][CH2:19][CH:18]([S:21]([C:24]4[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[CH:26][CH:25]=4)(=O)=O)[CH2:17][CH2:16]3)[O:11][C:10]2=[O:32])=[CH:5][CH:4]=1>CS(C)=O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH2:13][C@H:12]([CH2:14][N:15]3[CH2:20][CH2:19][CH:18]([S:21][C:24]4[CH:25]=[CH:26][C:27]([O:30][CH3:31])=[CH:28][CH:29]=4)[CH2:17][CH2:16]3)[O:11][C:10]2=[O:32])=[CH:7][CH:8]=1

Participants

3

Reactant 1

HCID 15228020HCID 15228020, compound

Product 1

HCID 54064094HCID 54064094, compound

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Procedure

3-p-methoxyphenyl-5(S)-[(4-p-methoxyphenylsulfonylpiperidino)methyl]-2-oxazolidinone (hydrochloride), m.p. 254°-256°; [αD =-31.6° (DMSO);

Sources & evidence

ORD record
ord-a4c7c4f8e6664269bd9189e64fa2ec91
Source dataset
uspto-grants-1996_10
Patent number
US05561145

Reaction notes

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