HCID 53271728, compound → HCID 66928143, compound

HRID 2065165Notes

Reaction equation

HRID 2065165 reaction equation
[CH3:1][C:2]1([C:7]2[O:11][C:10]([CH2:12][N:13]3[CH:17]=[C:16]([NH2:18])[CH:15]=[N:14]3)=[CH:9][CH:8]=2)[O:6]CCO1.[F:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[C:26]1[S:30][CH:29]=[N:28][C:27]=1[C:31](O)=[O:32]>>[C:2]([C:7]1[O:11][C:10]([CH2:12][N:13]2[CH:17]=[C:16]([NH:18][C:31]([C:27]3[N:28]=[CH:29][S:30][C:26]=3[C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=3[F:19])=[O:32])[CH:15]=[N:14]2)=[CH:9][CH:8]=1)(=[O:6])[CH3:1]

Participants

3

Reactant 2

HCID 53271728HCID 53271728, compoundHCID 669286111-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-4-ylamine

Product 1

HCID 66928143HCID 66928143, compound

Procedure

Following general procedure B followed by either C or D, starting from 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-4-ylamine and 5-(2-fluoro-phenyl)-thiazole-4-carboxylic acid.

Sources & evidence

ORD record
ord-c317d94143f34c3db55304d210b719d6
Source dataset
uspto-grants-2012_10
Patent number
US08288419B2

Reaction notes

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