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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519281Generated: October 27, 2026

2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-one → 4-[4-(5-Bromo-thiophen-2-yl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid

https://huagongshe.com/reaction/1519281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-oneHCID 1988398—
Reactant2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl esterHCID 86679832—
Product4-[4-(5-Bromo-thiophen-2-yl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acidHCID 7153663133%

Reaction Steps

4-[4-(5-Bromo-thiophen-2-yl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid (180 mg, 33%) was prepared from 2′-nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester (which may be prepared as described for Intermediate 4) and 2-bromo-1-(5-bromothiophen-2-yl)ethanone (available from Oakwood Products, Inc.) using the procedure described for the preparation of Example 1. 1H NMR (300 MHz, DMSO-d6) δ 13.16 (s, 1H), 8.50 (d, J=1.8 Hz, 1H), 8.13-8.22 (m, 3H), 7.52 (d, J=3.9 Hz, 1H), 7.40-7.48 (m, 2H), 7.28 (d, J=3.9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073881B2
Source datasetuspto-grants-2015_07
ORD IDord-986348c0c53a4cb4a5c4314be947742f
Source noteuspto-grants-2015_07