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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888915Generated: November 1, 2026

Benzothiazole → 5-Benzothiazol-2-yl-4'-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide

https://huagongshe.com/reaction/1888915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantTriphenylphosphineHCID 11776—
Reactant5-Iodo-4'-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amideHCID 59432537—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product5-Benzothiazol-2-yl-4'-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amideHCID 5943255997.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a stirred solution of 5-iodo-4′-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide (150 mg, 0.37 mmol) in 1 ml dry DMF were added CuI (15.24 mg, 20% eq), Pd(OAc)2 (4.2 mg, 5% eq), PPh3 (19.5 mg, 20% eq) and benzothiazole (63.5 mg, 1.5 eq) at room temperature. The reaction mixture was heated to 150° C. by microwave irridiation for 45 minutes. The reaction mixture was cooled and extracted with EtOAc, washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by preparative HPLC to give 5-benzothiazol-2-yl-4′-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide (150 mg, 60%). MS (M+H)=417.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501933B2
Source datasetuspto-grants-2013_08
ORD IDord-e6fae63fe3e64d60a0300421cbc0394e
Source noteuspto-grants-2013_08