5-Phenyl-1,3-oxazole-4-carboxylic acid → HCID 66929084, compound

HRID 2065341Notes

Reaction equation

HRID 2065341 reaction equation
[CH3:1][S:2]([C:5]1[O:9][C:8]([CH2:10][N:11]2[CH:15]=[C:14]([NH2:16])[CH:13]=[N:12]2)=[CH:7][CH:6]=1)(=[O:4])=[O:3].[C:17]1([C:23]2[O:27][CH:26]=[N:25][C:24]=2[C:28](O)=[O:29])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH3:1][S:2]([C:5]1[O:9][C:8]([CH2:10][N:11]2[CH:15]=[C:14]([NH:16][C:28]([C:24]3[N:25]=[CH:26][O:27][C:23]=3[C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)=[O:29])[CH:13]=[N:12]2)=[CH:7][CH:6]=1)(=[O:4])=[O:3]

Participants

3

Reactant 2

HCID 27762995-Phenyl-1,3-oxazole-4-carboxylic acidHCID 66929437HCID 66929437, compound

Product 1

HCID 66929084HCID 66929084, compound

Procedure

Following general procedure B followed by C, starting from 1-(5-methanesulfonyl-furan-2-ylmethyl)-1H-pyrazol-4-ylamine and 5-phenyl-oxazole-4-carboxylic acid. LC-MS-conditions 02: tR=0.94 min; [M+H]+=413.29.

Sources & evidence

ORD record
ord-1a9cda16068746e299aa3d25293680de
Source dataset
uspto-grants-2012_10
Patent number
US08288419B2

Reaction notes

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