5-(m-Tolyl)oxazole-4-carboxylic acid → HCID 66928686, compound

HRID 2065298Notes

Reaction equation

HRID 2065298 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.[CH3:19][C:20]1[CH:21]=[C:22]([C:26]2[O:30][CH:29]=[N:28][C:27]=2[C:31](O)=[O:32])[CH:23]=[CH:24][CH:25]=1>>[C:2]([C:7]1[O:11][C:10]([CH2:12][N:13]2[CH:17]=[CH:16][C:15]([NH:18][C:31]([C:27]3[N:28]=[CH:29][O:30][C:26]=3[C:22]3[CH:21]=[C:20]([CH3:19])[CH:25]=[CH:24][CH:23]=3)=[O:32])=[N:14]2)=[CH:9][CH:8]=1)(=[O:6])[CH3:1]

Participants

3

Reactant 2

HCID 299230925-(m-Tolyl)oxazole-4-carboxylic acidHCID 669287811-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine

Product 1

HCID 66928686HCID 66928686, compound

Procedure

Following general procedure B followed by T, starting from 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine and 5-(3-methyl-phenyl)-oxazole-4-carboxylic acid. LC-MS-conditions 02: tR=1.01 min; [M+H]+=391.5.

Sources & evidence

ORD record
ord-ceb2ef94b88740b4b189cc436bc22e89
Source dataset
uspto-grants-2012_10
Patent number
US08288419B2

Reaction notes

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