HCID 178503094, compound → HCID 178503095, compound

HRID 2064590Notes

Reaction equation

HRID 2064590 reaction equation
[CH3:1][S:2][C:3]1[NH:7][N:6]=[C:5]([C:8]2[N:12](COCC[Si](C)(C)C)[C:11]3[CH:21]=[CH:22][C:23]([C:25]([F:28])([F:27])[F:26])=[CH:24][C:10]=3[N:9]=2)[CH:4]=1.CSC1NN=C(N2C3C=CC(C(F)(F)F)=CC=3N=C2)C=1>>[CH3:1][S:2][C:3]1[NH:7][N:6]=[C:5]([C:8]2[NH:12][C:11]3[CH:21]=[CH:22][C:23]([C:25]([F:28])([F:26])[F:27])=[CH:24][C:10]=3[N:9]=2)[CH:4]=1

Participants

3

Reactant 2

HCID 178503094HCID 178503094, compoundHCID 178503289HCID 178503289, compound

Product 1

HCID 178503095HCID 178503095, compound

Procedure

By proceeding in a similar manner to Example 230(a) above but using 2-(5-methylsulfanyl-1H-pyrazol-3-yl)-5-trifluoromethyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazole [Reference Example 1(d)] there was prepared 2-(5-methylsulfanyl-1H-pyrazol-3-yl-5-trifluoromethyl-1H-benzoimidazole.

Sources & evidence

ORD record
ord-6cc53ffeab6041b2be8e6885c90d470e
Source dataset
uspto-grants-2012_10
Patent number
US08288425B2

Reaction notes

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