HCID 23146349, compound → HCID 23146332, compound

HRID 1367046Notes

Reaction equation

HRID 1367046 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([CH2:10][CH:11]3[CH2:16][N:15](C)[CH2:14][CH2:13][N:12]3[C:18]([C:20]3[N:21]=[C:22]([CH3:32])[S:23][C:24]=3[C:25]3[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=3)=[O:19])=[CH:7][C:6]=2[CH:33]=1.C1C=C2C(N/N=C3/C4C=CC(S([O-])(=O)=O)=CC=4C=C(S([O-])(=O)=O)C/3=O)=CC=C(S([O-])(=O)=O)C2=CC=1.[Na+].[Na+].[Na+]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([CH2:10][CH:11]3[CH2:16][NH:15][CH2:14][CH2:13][N:12]3[C:18]([C:20]3[N:21]=[C:22]([CH3:32])[S:23][C:24]=3[C:25]3[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=3)=[O:19])=[CH:7][C:6]=2[CH:33]=1

Participants

3

Reactant 2

HCID 23146349HCID 23146349, compoundHCID 178516958HCID 178516958, compound

Product 1

HCID 23146332HCID 23146332, compound

Procedure

The title compound was prepared from 1-[2-(5-chloro-benzofuran-2-ylmethyl)-4-methyl-piperazin-1-yl]-1-[5-(4-fluoro-phenyl)-2-methyl-thiazol-4-yl]-methanone, E123 (95 mg) by a procedure similar to that described for Example 85.

Sources & evidence

ORD record
ord-c42542e962944a38b87c4998e1d61372
Source dataset
uspto-grants-2011_02
Patent number
US07893090B2

Reaction notes

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