HCID 59587542, compound → HCID 66928540, compound

HRID 2065205Notes

Reaction equation

HRID 2065205 reaction equation
[F:1][C:2]([F:14])([CH3:13])[CH2:3][CH2:4][CH2:5][CH2:6][N:7]1[CH:11]=[C:10]([NH2:12])[CH:9]=[N:8]1.[CH3:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([C:23]2[O:27][C:26]([CH3:28])=[N:25][C:24]=2[C:29](O)=[O:30])=[CH:19][CH:18]=1>>[F:14][C:2]([F:1])([CH3:13])[CH2:3][CH2:4][CH2:5][CH2:6][N:7]1[CH:11]=[C:10]([NH:12][C:29]([C:24]2[N:25]=[C:26]([CH3:28])[O:27][C:23]=2[C:20]2[CH:21]=[CH:22][C:17]([O:16][CH3:15])=[CH:18][CH:19]=2)=[O:30])[CH:9]=[N:8]1

Participants

3

Reactant 2

HCID 59587542HCID 59587542, compoundHCID 669291721-(5,5-Difluoro-hexyl)-1H-pyrazol-4-ylamine

Product 1

HCID 66928540HCID 66928540, compound

Procedure

Following general procedure B, starting from 1-(5,5-difluoro-hexyl)-1H-pyrazol-4-ylamine and 5-(4-methoxy-phenyl)-2-methyl-oxazole-4-carboxylic acid. LC-MS-conditions 05b: tR=1.14 min; [M+H]+=419.26.

Sources & evidence

ORD record
ord-daa13337370c4f129293c59d9fc299e4
Source dataset
uspto-grants-2012_10
Patent number
US08288419B2

Reaction notes

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