HCID 43263136, compound → HCID 59301358, compound

HRID 2236261Notes

Reaction equation

HRID 2236261 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[O:9][C:10]([C:16]([F:19])([F:18])[F:17])=[C:11]([C:13]([OH:15])=O)[N:12]=1.[CH2:20]([N:22]([CH3:30])[C:23]1[CH:28]=[CH:27][C:26]([NH2:29])=[CH:25][N:24]=1)[CH3:21]>>[CH2:20]([N:22]([CH3:30])[C:23]1[N:24]=[CH:25][C:26]([NH:29][C:13]([C:11]2[N:12]=[C:8]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[Br:1])[O:9][C:10]=2[C:16]([F:19])([F:18])[F:17])=[O:15])=[CH:27][CH:28]=1)[CH3:21]

Participants

3

Reactant 2

HCID 43263136HCID 43263136, compoundHCID 59301376HCID 59301376, compound

Product 1

HCID 59301358HCID 59301358, compound

Procedure

With a procedure similar to example 16 above, 2-(2-bromo-phenyl)-5-trifluoromethyl-oxazole-4-carboxylic acid [6-(ethyl-methyl-amino)-pyridin-3-yl]-amide was prepared from 2-(2-bromo-phenyl)-5-trifluoromethyl-oxazole-4-carboxylic acid and N2-ethyl-N2-methyl-pyridine-2,5-diamine. LCMS calcd for C19H16BrF3N4O2 (m/e) 469, obsd 470 (M+H).

Sources & evidence

ORD record
ord-af40b3b687b5470684998f2e98eb2bd2
Source dataset
uspto-grants-2010_05
Patent number
US07714126B2

Reaction notes

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