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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098061Generated: November 1, 2026

2-(3,3-Difluoro-2-oxoindolin-1-yl)acetic acid → N-(4-bromo-3-(4H-1,2,4-triazol-3-yl)thiophen-2-yl)-2-(3,3-difluoro-2-oxoindolin-1-yl)acetamide

https://huagongshe.com/reaction/2098061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3,3-Difluoro-2-oxoindolin-1-yl)acetic acidHCID 68755194—
ReactantHCID 178509325HCID 178509325—
ProductN-(4-bromo-3-(4H-1,2,4-triazol-3-yl)thiophen-2-yl)-2-(3,3-difluoro-2-oxoindolin-1-yl)acetamideHCID 17852125514.7%

Reaction Steps

The title compound was prepared from 2-(3,3-difluoro-2-oxoindolin-1-yl)acetic acid (50 mg, 0.22 mmol), 4-bromo-3-(4H-1,2,4-triazol-3-yl)thiophen-2-amine (45 mg, 0.18 mmol) using protocol A. HPLC purification gave N-(4-bromo-3-(4H-1,2,4-triazol-3-yl)thiophen-2-yl)-2-(3,3-difluoro-2-oxoindolin-1-yl)acetamide (12 mg) as a white solid (m/z 454.0, retention of 5.696 min in [7]). 1H-NMR (300 MHz, CDCl3) δ 13.1 (s, 1H), 7.82 (s, 1H), 7.70 (dd, J=7.5, 1.5 Hz, 1H), 7.50 (td, J=7.9, 1.2 Hz, 1H), 6.99 (s, 1H), 6.92 (d, J=7.9 Hz, 1H), 4.71 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-84482c4fb1aa4077be2a8f0cfa7b6b08
Source noteuspto-grants-2013_05