Dimethyl Sulfoxide → HCID 22337876, compound

HRID 585594Notes

Reaction equation

HRID 585594 reaction equation
Br[C:2]1[CH:27]=[CH:26][C:5]([CH2:6][O:7][C:8]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:9]=2[CH:10]=[CH:11][C:12]([NH:18][S:19]([C:22]([F:25])([F:24])[F:23])(=[O:21])=[O:20])=[CH:13]3)=[CH:4][CH:3]=1.[Cl:28][C:29]1[CH:30]=[C:31](B(O)O)[CH:32]=[C:33]([Cl:35])[CH:34]=1.CS(C)=O>O>[Cl:28][C:29]1[CH:30]=[C:31]([C:2]2[CH:27]=[CH:26][C:5]([CH2:6][O:7][C:8]3[CH:17]=[CH:16][CH:15]=[C:14]4[C:9]=3[CH:10]=[CH:11][C:12]([NH:18][S:19]([C:22]([F:24])([F:23])[F:25])(=[O:21])=[O:20])=[CH:13]4)=[CH:4][CH:3]=2)[CH:32]=[C:33]([Cl:35])[CH:34]=1

Participants

5

Reactant 3

HCID 679Dimethyl SulfoxideHCID 27343313,5-Dichlorophenylboronic acidHCID 22337880HCID 22337880, compound

Product 1

HCID 22337876HCID 22337876, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The title compound was prepared from the product of Example 1 and 3,5-dichloro phenyl boronic acid according to the procedure of Example 2, m.p. 138-140 DMSO: δ 12.1(s, 1H), 7.0-8.3(m, 13H, arom), 5.38 (s, 2H). CHN 53.84, 3.20, 2.62 (0.5 M H2O) Found 53.97, 3.02, 2.40.

Sources & evidence

ORD record
ord-c6959957f1664b8580480eabceccf208
Source dataset
uspto-grants-2005_08
Patent number
US06933322B2

Reaction notes

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