2-Phenyl-5-(trifluoromethyl)-oxazole-4-carboxylic acid → HCID 57393260, compound

HRID 2236277Notes

Reaction equation

HRID 2236277 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.[NH2:19][C:20]1[CH:21]=[CH:22][C:23]([N:26]([CH3:30])[CH2:27][CH2:28][OH:29])=[N:24][CH:25]=1>>[OH:29][CH2:28][CH2:27][N:26]([CH3:30])[C:23]1[N:24]=[CH:25][C:20]([NH:19][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:21][CH:22]=1

Participants

3

Reactant 2

HCID 27764382-Phenyl-5-(trifluoromethyl)-oxazole-4-carboxylic acidHCID 226936302-[(5-Amino-2-pyridinyl)methylamino]ethanol

Product 1

HCID 57393260HCID 57393260, compound

Procedure

With a procedure similar to example 43 above, 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid {6-[(2-hydroxy-ethyl)-methyl-amino]-pyridin-3-yl}-amide was prepared from 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid and 2-[(5-amino-pyridin-2-yl)-methyl-amino]-ethanol. LCMS calcd for C19H17F3N4O3 (m/e) 406, obsd 407 (M+H).

Sources & evidence

ORD record
ord-a0f8bf90abcf4153840260482a289e1c
Source dataset
uspto-grants-2010_05
Patent number
US07714126B2

Reaction notes

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