1-Methyl-3-aminopyrazole → HCID 23160282, compound

HRID 2246345Notes

Reaction equation

HRID 2246345 reaction equation
F[C:2]1[C:7]([C:8]([F:11])([F:10])[F:9])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:12][OH:13].[NH2:14][C:15]1[CH:19]=[CH:18][N:17]([CH3:20])[N:16]=1.Cl[C:22]1[C:31]2[C:26](=[CH:27][CH:28]=[C:29]([OH:32])[CH:30]=2)[N:25]=[CH:24][N:23]=1>>[CH3:20][N:17]1[CH:18]=[CH:19][C:15]([NH:14][C:22]2[C:31]3[C:26](=[CH:27][CH:28]=[C:29]([O:32][C:2]4[C:7]([C:8]([F:11])([F:10])[F:9])=[CH:6][CH:5]=[CH:4][C:3]=4[CH2:12][OH:13])[CH:30]=3)[N:25]=[CH:24][N:23]=2)=[N:16]1

Participants

4

Reactant 3

HCID 1372541-Methyl-3-aminopyrazoleHCID 5893612-Fluoro-3-(trifluoromethyl)benzyl alcoholHCID 231602734-Chloroquinazolin-6-ol

Product 1

HCID 23160282HCID 23160282, compound

Procedure

The compound of Example 142 was manufactured by the same method as in Example 95, by a similar method thereto or by a combination of such a method with a conventional method using 2-fluoro-3-(trifluoromethyl)-benzenemethanol, 3-amino-1-methyl-1H-pyrazole and 4-chloro-6-hydroxy-quinazoline.

Sources & evidence

ORD record
ord-3468ee41c6b845928a1d28e15fe3dd62
Source dataset
uspto-grants-2010_03
Patent number
US07687502B2

Reaction notes

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