HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356692Generated: November 1, 2026
2,4-Difluoroaniline → HCID 57829267, compound
https://huagongshe.com/reaction/2356692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | 4-Amino-2-chlorobenzonitrile | HCID 88728 | — |
| Reactant | HCID 68676578 | HCID 68676578 | — |
| Reactant | HCID 68676731 | HCID 68676731 | — |
| Product | HCID 57829267 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759366B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-f65a7fd6c7784955b5c6cacafff69aba |
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| Source note | uspto-grants-2010_07 |
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