N2,N2-dimethylpyridine-2,5-diamine → HCID 59301462, compound

HRID 2236242Notes

Reaction equation

HRID 2236242 reaction equation
[C:1]1([C:7]2[O:8][C:9]([C:15]([F:18])([F:17])[F:16])=[C:10]([C:12]([OH:14])=O)[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:19][N:20]([CH3:28])[C:21]1[CH:26]=[CH:25][C:24]([NH2:27])=[CH:23][N:22]=1>>[CH3:19][N:20]([CH3:28])[C:21]1[N:22]=[CH:23][C:24]([NH:27][C:12]([C:10]2[N:11]=[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[O:8][C:9]=2[C:15]([F:18])([F:17])[F:16])=[O:14])=[CH:25][CH:26]=1

Participants

3

Reactant 2

HCID 78642N2,N2-dimethylpyridine-2,5-diamineHCID 27764382-Phenyl-5-(trifluoromethyl)-oxazole-4-carboxylic acid

Product 1

HCID 59301462HCID 59301462, compound

Procedure

With a procedure similar to the example 1 above, 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (6-dimethylamino-pyridin-3-yl)-amide was prepared from 2-phenyl-trifluoromethyl-oxazole-4-carboxylic acid and N2,N2-dimethyl-pyridine-2,5-diamine. LCMS calcd for C18H15F3N4O2 (m/e) 376.34 obsd 377.12 (M+H).

Sources & evidence

ORD record
ord-c9d401729a0044569f8bc55f2be514bd
Source dataset
uspto-grants-2010_05
Patent number
US07714126B2

Reaction notes

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