HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243124Generated: October 28, 2026
Trifluoroacetic acid → (S)-1-(6-Fluoro-1-isopropyl-1H-benzoimidazol-2-yl)ethylamine
https://huagongshe.com/reaction/243124
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | [(S)-1-(6-Fluoro-1-isopropyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid tert-butyl ester | HCID 68179453 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-1-(6-Fluoro-1-isopropyl-1H-benzoimidazol-2-yl)ethylamine | HCID 68157766 | 72.7% |
Reaction Steps
[(S)-1-(6-Fluoro-1-isopropyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid tert-butyl ester (1.0 g, 3.11 mmol) was dissolved in DCM (10 mL) and TFA (5 mL) added. The reaction mixture was stirred at RT for 30 minutes. The resultant mixture was concentrated in vacuo and the residue dissolved in DCM (40 mL) and stirred vigorously with saturated aqueous NaHCO3 (20 mL), for 10 minutes. The layers were separated and the organic fraction washed with brine (20 mL), dried (MgSO4), filtered and concentrated in vacuo to afford the title compound (0.5 g, 72%). 1H NMR (CDCl3, 400 MHz): δ 7.65 (1H, dd, J=8.83, 5.01 Hz), 7.20 (1H, dd, J=9.40, 2.46 Hz), 6.97 (1H, ddd, J=9.58, 8.80, 2.43 Hz), 4.92-4.82 (1H, m), 4.37-4.28 (1H, q, J=6.68 Hz), 1.64 (6H, d, J=6.98 Hz), 1.58 (3H, d, J=6.65 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-0d5a628df1fc4180905366518bb60287 |
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| Source note | uspto-grants-2014_02 |
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