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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250934Generated: November 1, 2026

Sodium Carbonate → thiophene-3-carboxylic acid N'-[2-(5-fluoro-2'-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N'-isopropyl hydrazide

https://huagongshe.com/reaction/2250934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2777204—
ReactantThiophene-3-carboxylic acid n'-[2-(2-bromo-4-fluoro-phenoxy)-acetyl]-n'-isopropyl-hydrazidHCID 58689906—
Solvent1,2-DimethoxyethaneHCID 8071—
Productthiophene-3-carboxylic acid N'-[2-(5-fluoro-2'-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N'-isopropyl hydrazideHCID 1169891863.1%

Reaction Steps

A solution of thiophene-3-carboxylic acid N′-[2-(2-bromo-4-fluoro-phenoxy)-acetyl]-N′-isopropyl-hydrazide (251 mg, 0.60 mmol) in DME (5 ml)/2M Na2CO3 (1.05 ml, 2.12 mmol) was with 2-trifluoromethoxyphenylboronic acid (187 mg, 0.91 mmol) and Pd[PPh3]4 (140 mg, 0.12 mmol) in a microwave oven at 150° C. for 10 min. The reaction mixture was partitioned between water and DCM. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated. The crude was adsorbed on silica and purified on a silica gel column with a 30-50% ethyl acetate/hexane gradient to afford the product as a solid (188 mg, 63%). MS m/e 497.41 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317125B2
Source datasetuspto-grants-2008_01
ORD IDord-09b65af868e14057a9f27678b678b667
Source noteuspto-grants-2008_01