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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356692Generated: November 1, 2026

2,4-Difluoroaniline → HCID 57829267, compound

https://huagongshe.com/reaction/2356692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluoroanilineHCID 9709—
Reactant4-Amino-2-chlorobenzonitrileHCID 88728—
ReactantHCID 68676578HCID 68676578—
ReactantHCID 68676731HCID 68676731—
ProductHCID 57829267HCID 57829267—

Reaction Steps

The compound of Example 253 (5-{3-[2-(2,4-difluorophenylamino)-4-fluorobenzyl]-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl}-4′-fluorobiphenyl-2-carbonitrile, molecular weight 558.16 (C31H22F4N4O2); retention time Rt=2.38 min. [B]; MS (ESI): 559.15 (MH+)) was obtained similarly to the manner described for the preparation of the compound of Example 223 via the sequence of 4-amino-2-chlorobenzonitrile→5-amino-4′-fluorobiphenyl-2-carbonitrile (253.3, 1H NMR: 7.54-7.49, m, 3H, 7.31, t, 2H, 6.61, m, 2H, 6.25, s, 2H)→5-(4,4-dimethyl-2,5-dioxoimidazolidin-1-yl)-4′-fluorobiphenyl-2-carbonitrile (253.1, 1H NMR: 8.73, s, 1H; 8.09, d, 1H, 7.74, s, 1H, 7.65, m, 3H, 7.41, m, 2H, 1.42, s, 6H)→5-[3-(2-bromo-4-fluorobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-4′-fluorobiphenyl-2-carbonitrile (253.2, 1H NMR: 8.1, d, 1H, 7.8, s, 1H, 7.75, d, 1H, 7.69-7.59, m, 4H; 7.41, t, 1H, 4.61, s, 2H, 1.4, s, 6H) δ 253 (from 253.2 by reaction with 2,4-difluorophenylamine).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759366B2
Source datasetuspto-grants-2010_07
ORD IDord-f65a7fd6c7784955b5c6cacafff69aba
Source noteuspto-grants-2010_07