Potassium Carbonate → HCID 86602303, compound

HRID 1821976Notes

Reaction equation

HRID 1821976 reaction equation
[CH3:1][C:2]1[N:3]=[C:4]([C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=2)[S:5][CH:6]=1.[Cl:14][C:15]1[CH:29]=[C:28]([O:30][CH2:31][CH:32]=[C:33]([Cl:35])[Cl:34])[CH:27]=[C:26]([Cl:36])[C:16]=1[O:17][CH2:18][CH2:19][CH2:20]OS(C)(=O)=O.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Cl:14][C:15]1[CH:29]=[C:28]([O:30][CH2:31][CH:32]=[C:33]([Cl:35])[Cl:34])[CH:27]=[C:26]([Cl:36])[C:16]=1[O:17][CH2:18][CH2:19][CH2:20][O:13][C:10]1[CH:11]=[CH:12][C:7]([C:4]2[S:5][CH:6]=[C:2]([CH3:1])[N:3]=2)=[CH:8][CH:9]=1

Participants

5

Procedure

96 mg of 4-(4-methyl-thiazol-2-yl)-phenol, 212 mg of methanesulfonic acid 3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propyl ester and 207 mg of potassium carbonate are stirred for 24 hours at 50° C. in 3 ml of dimethylformamide. The reaction mixture is poured onto water and extracted with ethyl acetate. Concentration of the organic phase and purification over silica gel yield the title compound (compound 1.23).

Workup

  1. additionThe reaction mixture is poured onto water
  2. extractionextracted with ethyl acetate
  3. customConcentration of the organic phase and purification over silica gel

Sources & evidence

ORD record
ord-67f5016dbc294decb62f271d8e5446ce
Source dataset
uspto-grants-2009_10
Patent number
US07608631B2

Reaction notes

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