Potassium Carbonate → Methyl 2-[5-chloro-2-[4-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)phenylthiomethyl]phenoxy]propanoate

HRID 343287Notes

Reaction equation

HRID 343287 reaction equation
[Cl:1][C:2]1[C:3]([C:12]2[CH:17]=[CH:16][C:15]([SH:18])=[CH:14][CH:13]=2)=[N:4][N:5]([CH3:11])[C:6]=1[O:7][CH:8]([F:10])[F:9].[Cl:19][C:20]1[CH:21]=[CH:22][C:23]([CH2:33]Cl)=[C:24]([CH:32]=1)[O:25][CH:26]([CH3:31])[C:27]([O:29][CH3:30])=[O:28].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Cl:19][C:20]1[CH:21]=[CH:22][C:23]([CH2:33][S:18][C:15]2[CH:16]=[CH:17][C:12]([C:3]3[C:2]([Cl:1])=[C:6]([O:7][CH:8]([F:9])[F:10])[N:5]([CH3:11])[N:4]=3)=[CH:13][CH:14]=2)=[C:24]([CH:32]=1)[O:25][CH:26]([CH3:31])[C:27]([O:29][CH3:30])=[O:28]

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 53768369Methyl 2-(2-chloromethyl-5-chlorophenoxy)propionateHCID 1359608844-(4-Chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)thiophenol

Product 1

HCID 67703361Methyl 2-[5-chloro-2-[4-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)phenylthiomethyl]phenoxy]propanoate

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

This compound is prepared in a manner analogous to that of Step I of Example 1, using 0.58 gram (0.002 mole) of 4-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)thiophenol, 0.32 gram (0.002 mole) of methyl 2-(5-chloro-2-chloromethylphenoxy)propanoate (prepared as in Steps A through D of Example 2), and 0.41 gram (0.003 mole) of potassium carbonate in 60 mil of N,N-di-methylformamide, yielding the title compound.

Workup

  1. customThis compound is prepared in a manner analogous to that of Step I of Example 1

Sources & evidence

ORD record
ord-9a7c099280614c60a3dab91b2277e432
Source dataset
uspto-grants-1999_01
Patent number
US05861359

Reaction notes

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