Sodium Hydroxide → HCID 19738055, compound

HRID 2255391Notes

Reaction equation

HRID 2255391 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([CH2:12][CH2:13][CH2:14][N:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)[C:10]#[N:11].Cl.Cl[CH2:23][N:24]1[CH:28]=[N:27][CH:26]=[N:25]1.[OH-].[Na+]>CS(C)=O>[C:10]([C:9]([C:3]1[CH:4]=[CH:5][C:6]([Cl:8])=[CH:7][C:2]=1[Cl:1])([CH2:12][CH2:13][CH2:14][N:15]1[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]1)[CH2:23][N:24]1[CH:28]=[N:27][CH:26]=[N:25]1)#[N:11]

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 13268168HCID 13268168, compoundHCID 19738030HCID 19738030, compound

Product 1

HCID 19738055HCID 19738055, compound

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Procedure

This compound (5.0 g.) was prepared using the procedure described in Example 9b except using 5.0 g. (0.016 mole) of 2-(2,4-dichlorophenyl)-5-(1-piperidinyl)valeronitrile, 2.7 g. (0.0176 mole) of 1-(chloromethyl)-1,2,4-triazole hydrochloride, 3.2 g. (0.040 mole) of aqueous 50% sodium hydroxide, and 50 ml. of DMSO and was isolated as an oil.

Workup

  1. customThis compound (5.0 g.) was prepared

Sources & evidence

ORD record
ord-a42a472f92a34632906b6551c07b07c3
Source dataset
uspto-grants-1993_08
Patent number
US05240925

Reaction notes

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