HCID 23567177, compound → HCID 20766018, compound

HRID 984102Notes

Reaction equation

HRID 984102 reaction equation
[CH3:1][O:2][C:3]([CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[C:10]([S:15](Cl)(=O)=O)[CH:11]=2)[O:6]1)=[O:4].COC(C1C=CC2C=C(SCC3SC(C4C=CC(C(F)(F)F)=CC=4)=NC=3C)C=CC=2O1)=O>>[CH3:1][O:2][C:3]([CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[C:10]([SH:15])[CH:11]=2)[O:6]1)=[O:4]

Participants

3

Reactant 2

HCID 23567177HCID 23567177, compoundHCID 69590777HCID 69590777, compound2×

Product 1

HCID 20766018HCID 20766018, compound

Procedure

Compound 3C was prepared according to the method of Example 1 utilizing compound 3B. Compound 3C was prepared in 67% yield. MS: 223 (M−1)+. Preparation of 6-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethylsulfanyl]-1-benzopyran-2-carboxylic acid methyl ester (Compound 3D)

Workup

  1. customCompound 3C was prepared

Sources & evidence

ORD record
ord-ce1a4aca93ac45f6b5040c6468e73246
Source dataset
uspto-grants-2005_03
Patent number
US06867224B2

Reaction notes

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