HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092212Generated: November 2, 2026
Ethyl Acetate → 3-(5-Cyclopropyl-1H-pyrazol-3-yl)-4,6-difluoro-N-((S)-1-(4-fluorophenyl)ethyl)-3H-benzo[d]imidazol-5-amine
https://huagongshe.com/reaction/1092212
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (S)-N3-(5-Cyclopropyl-1H-pyrazol-3-yl)-2,6-difluoro-N1-(1-(4-fluorophenyl)ethyl)benzene-1,3,4-triamine | HCID 86621763 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(5-Cyclopropyl-1H-pyrazol-3-yl)-4,6-difluoro-N-((S)-1-(4-fluorophenyl)ethyl)-3H-benzo[d]imidazol-5-amine | HCID 66589200 | — |
Reaction Steps
(S)-N3-(5-Cyclopropyl-1H-pyrazol-3-yl)-2,6-difluoro-N1-(1-(4-fluorophenyl)ethyl)benzene-1,3,4-triamine (Method 101, 0.278 g, 0.718 mmol) and formamidine acetate (0.149 g, 1.44 mmol) in EtOH (10 ml) was heated at reflux for 1 hour. Saturated sodium bicarbonate solution (5 ml) and EtOAc (15 ml) were added. The organic layer was separated, washed with brine (3 ml) and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by chromatography (Hex-EtOAc=1:1) to give the title compound as off white solid (0.120 g, 42%). 1H NMR (400 MHz) 12.83 (s, 1H), 8.20 (s, 1H), 7.36 (m, 2H), 7.31 (d, J=11.2 Hz, 1H), 7.06 (t, J=8.8 Hz, 2H), 6.15 (s, 1H), 5.15 (d, J=10.4 Hz, 1H), 4.67 (m, 1H), 1.98 (m, 1H), 1.46 (d, J=6.8 Hz, 3H), 1.00 (m, 2H), 0.76 (m, 2H). MS: Calcd.: 397; Found: [M+H]+ 398.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129403B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-fe9214a35ade4953a6de62f03e2bbfa6 |
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| Source note | uspto-grants-2012_03 |
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