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1-Methyl-3-aminopyrazole → HCID 23160293, compound

HRID 2246332
Notes
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Reaction equation

HRID 2246332 reaction equation
Cl[C:2]1[C:7]([CH2:8][F:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[NH2:10][C:11]1[CH:15]=[CH:14][N:13]([CH3:16])[N:12]=1.Cl[C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([OH:28])[CH:26]=2)[N:21]=[CH:20][N:19]=1>>[F:9][CH2:8][C:7]1[C:2]([O:28][C:25]2[CH:26]=[C:27]3[C:22](=[CH:23][CH:24]=2)[N:21]=[CH:20][N:19]=[C:18]3[NH:10][C:11]2[CH:15]=[CH:14][N:13]([CH3:16])[N:12]=2)=[N:3][CH:4]=[CH:5][CH:6]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 1372541-Methyl-3-aminopyrazoleHCID 231602734-Chloroquinazolin-6-olHCID 231603702-Chloro-3-(fluoromethyl)pyridine

Product 1

HCID 23160293HCID 23160293, compound

Procedure

The compound of Example 125 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-chloro-3-fluoromethylpyridine, 3-amino-1-methyl-1H-pyrazole and 4-chloro-6-hydroxy-quinazoline.

Sources & evidence

ORD record
ord-1e4e23790b2b4e21b727d8c5a4956282
Source dataset
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07687502B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes