1-Methylindole-2-carboxaldehyde → HCID 11855082, compound

HRID 643324Notes

Reaction equation

HRID 643324 reaction equation
[CH2:1]([C:8]1[N:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:25])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:26][N:27]1[C:35]2[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH:29]=[C:28]1[CH:36]=O>>[CH2:1]([C:8]1[N:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH:24][CH2:36][C:28]3[N:27]([CH3:26])[C:35]4[C:30]([CH:29]=3)=[CH:31][CH:32]=[CH:33][CH:34]=4)[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:25])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 2671641-Methylindole-2-carboxaldehydeHCID 11855621[3-(3-Benzyl-8-chlorocinnolin-4-yl)phenyl]amine

Product 1

HCID 11855082HCID 11855082, compound

Procedure

The title compound was prepared from [3-(3-benzyl-8-chlorocinnolin-4-yl)phenyl]amine and 1-methyl-1H-indole-2-carbaldehyde according to the procedure of Step 5 Example 6. MS (ES) m/z 489.1.

Sources & evidence

ORD record
ord-dcc29c1467184ebfa06de27cb7de49f1
Source dataset
uspto-grants-2010_04
Patent number
US07700595B2

Reaction notes

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