Imidazole → HCID 9843286, compound

HRID 1635818Notes

Reaction equation

HRID 1635818 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6](F)[CH:5]=[CH:4][C:3]=1[C:9]([N:11]1[C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=2[CH2:15][N:14]2[CH:22]=[CH:23][CH:24]=[C:13]2[CH2:12]1)=[O:10].[H-].[Na+].CCCCCC.[NH:33]1[CH:37]=[CH:36][N:35]=[CH:34]1>CN(C)C=O>[Cl:1][C:2]1[CH:7]=[C:6]([N:33]2[CH:37]=[CH:36][N:35]=[CH:34]2)[CH:5]=[CH:4][C:3]=1[C:9]([N:11]1[C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=2[CH2:15][N:14]2[CH:22]=[CH:23][CH:24]=[C:13]2[CH2:12]1)=[O:10]

Participants

6

Reactant 4

HCID 795ImidazoleHCID 8058HexaneHCID 24758Sodium hydrideHCID 9798048HCID 9798048, compound

Product 1

HCID 9843286HCID 9843286, compoundYield 25%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

In the manner of Example 9's Method 1, employing (2-chloro-4-fluorophenyl)-(5H,11H-pyrrolo[2,1-c][1,4]benzodiazepin-10-yl)-methanone (2.0 g), 60% sodium hydride in oil (0.50 g, degreased with hexane), imidazole (0.50 g) and dimethylformamide (25 ml), the tide compound (0.57 g) was obtained as a tan amorphous solid, MS, n/z: 389 (M+H)+.

Sources & evidence

ORD record
ord-4c3c749af7854482bd63d16ddd66cf3b
Source dataset
uspto-grants-2003_01
Patent number
US06511974B1

Reaction notes

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