5-(3-Isopropoxymethyl-phenyl)-oxazole-4-carboxylic acid → HCID 66928365, compound

HRID 2065356Notes

Reaction equation

HRID 2065356 reaction equation
[CH3:1][C:2]1([C:7]2[O:11][C:10]([CH2:12][N:13]3[CH:17]=[CH:16][C:15]([NH2:18])=[N:14]3)=[CH:9][CH:8]=2)[O:6]CCO1.[CH:19]([O:22][CH2:23][C:24]1[CH:25]=[C:26]([C:30]2[O:34][CH:33]=[N:32][C:31]=2[C:35](O)=[O:36])[CH:27]=[CH:28][CH:29]=1)([CH3:21])[CH3:20]>>[C:2]([C:7]1[O:11][C:10]([CH2:12][N:13]2[CH:17]=[CH:16][C:15]([NH:18][C:35]([C:31]3[N:32]=[CH:33][O:34][C:30]=3[C:26]3[CH:27]=[CH:28][CH:29]=[C:24]([CH2:23][O:22][CH:19]([CH3:21])[CH3:20])[CH:25]=3)=[O:36])=[N:14]2)=[CH:9][CH:8]=1)(=[O:6])[CH3:1]

Participants

3

Procedure

Following general procedure B followed by C, starting from 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine and 5-(3-isopropoxymethyl-phenyl)-oxazole-4-carboxylic acid. LC-MS-conditions 02: tR=1.03 min; [M+H]+=449.63.

Sources & evidence

ORD record
ord-779d96b06680441ca18b72b34130e7dc
Source dataset
uspto-grants-2012_10
Patent number
US08288419B2

Reaction notes

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