Sodium hydride → HCID 19738039, compound

HRID 2255378Notes

Reaction equation

HRID 2255378 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:11][CH2:12][CH2:13][CH2:14][N:15]2[CH2:20][CH:19]([CH3:21])[O:18][CH:17]([CH3:22])[CH2:16]2)[C:9]#[N:10])=[CH:4][CH:3]=1.[H-].[Na+].Cl[CH2:26][N:27]1[CH:31]=[N:30][CH:29]=[N:28]1>CN(C=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:9]#[N:10])([CH2:11][CH2:12][CH2:13][CH2:14][N:15]2[CH2:16][CH:17]([CH3:22])[O:18][CH:19]([CH3:21])[CH2:20]2)[CH2:26][N:27]2[CH:31]=[N:30][CH:29]=[N:28]2)=[CH:4][CH:3]=1

Participants

5

Reactant 3

HCID 24758Sodium hydrideHCID 37438821-Chloromethyl-1H-1,2,4-triazoleHCID 53704383HCID 53704383, compound

Product 1

HCID 19738039HCID 19738039, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

This compound (400 mg.) was prepared using the procedure described in Example 2b except using 400 mg. (1.25 mmoles) of 2-(4-chlorophenyl)-6-(2,6-dimethyl-4-morpholinyl)capronitrile, 0.06 g. (1.38 mmoles) of sodium hydride, 0.15 g. (1.25 mmoles) of 1-(chloromethyl)-1,2,4-triazole, and 4 ml. of DMF and was isolated as a yellow oil.

Workup

  1. customThis compound (400 mg.) was prepared

Sources & evidence

ORD record
ord-140f902fc8044903b9d45f86c4a8c1ad
Source dataset
uspto-grants-1993_08
Patent number
US05240925

Reaction notes

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