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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888916Generated: October 26, 2026

4-Methylthiazole → 4'-Methyl-5-(4-methyl-thiazol-5-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide

https://huagongshe.com/reaction/1888916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylthiazoleHCID 12748—
Reactant5-Iodo-4'-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amideHCID 59432537—
ReactantHCID 178476685HCID 178476685—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product4'-Methyl-5-(4-methyl-thiazol-5-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amideHCID 5943253380%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 5-iodo-4′-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide (0.41 g, 1 mmol) and 4-methylthiazole (5 mmol) in 4 ml of DMF was added Pd(PPh3)4 (0.03 mmol) and CH3COOK (0.198 g, 2 mmol). The reaction mixture were heated to 100° C. and stirred for 14 hours. The reaction mixture was cooled to room temperature and extracted with EtOAc. The combined organic layers were washed with water and brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel, eluting with n-hexanes/ethyl acetate (1:6) to give 4′-Methyl-5-(4-methyl-thiazol-5-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide (30 mg, 80%) as a light yellow solid, MS (M+H)=381.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501933B2
Source datasetuspto-grants-2013_08
ORD IDord-50143c39819140e7991c6e05fc5a7896
Source noteuspto-grants-2013_08