HCID 66928761, compound → HCID 66928917, compound

HRID 2065314Notes

Reaction equation

HRID 2065314 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][O:20][CH2:21][CH2:22][C:23]1[CH:24]=[C:25]([C:29]2[O:33][CH:32]=[N:31][C:30]=2[C:34](O)=[O:35])[CH:26]=[CH:27][CH:28]=1>>[C:2]([C:7]1[O:11][C:10]([CH2:12][N:13]2[CH:17]=[CH:16][C:15]([NH:18][C:34]([C:30]3[N:31]=[CH:32][O:33][C:29]=3[C:25]3[CH:26]=[CH:27][CH:28]=[C:23]([CH2:22][CH2:21][O:20][CH3:19])[CH:24]=3)=[O:35])=[N:14]2)=[CH:9][CH:8]=1)(=[O:6])[CH3:1]

Participants

3

Reactant 2

HCID 66928761HCID 66928761, compoundHCID 669287811-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine

Product 1

HCID 66928917HCID 66928917, compound

Procedure

Following general procedure B followed by C, 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine and 5-[3-(2-methoxy-ethyl)-phenyl]-oxazole-4-carboxylic acid. LC-MS-conditions 02: tR=0.98 min; [M+H]+=435.45.

Sources & evidence

ORD record
ord-73fbf85d077f482a9e99d8980e872aea
Source dataset
uspto-grants-2012_10
Patent number
US08288419B2

Reaction notes

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