HCID 66579312, compound → HCID 66577738, compound

HRID 1624418Notes

Reaction equation

HRID 1624418 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[CH:14]=[O:15])=[CH:4][CH:3]=1.[F:16][C:17]([F:31])([F:30])[C:18]1[CH:19]=[C:20]([CH:27]=[CH:28][CH:29]=1)[CH2:21][C:22]1[O:23][CH:24]=[N:25][N:26]=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[CH:14]([C:24]2[O:23][C:22]([CH2:21][C:20]3[CH:27]=[CH:28][CH:29]=[C:18]([C:17]([F:30])([F:31])[F:16])[CH:19]=3)=[N:26][N:25]=2)[OH:15])=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 66579312HCID 66579312, compoundHCID 821337925-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carbaldehyde

Product 1

HCID 66577738HCID 66577738, compound

Procedure

Prepared according to the procedure described in Example 19, Step 1, using 5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carbaldehyde and 2-(3-trifluoromethyl-benzyl)-[1,3,4]oxadiazole.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-531457a1332a49a79c399f68e8f7c1a8
Source dataset
uspto-grants-2014_07
Patent number
US08778983B2

Reaction notes

Loading…