HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450395Generated: October 26, 2026
Ethanol → N-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-3-(3-propan-2-yloxy-1H-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amine
https://huagongshe.com/reaction/450395
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | HCID 178458651 | HCID 178458651 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | N-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-3-(3-propan-2-yloxy-1H-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amine | HCID 178458590 | — |
Reaction Steps
N6-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-N2-(5-isopropoxy-1H-pyrazol-3-yl)-3-nitropyridine-2,6-diamine (Intermediate 8, 0.5 g) was dissolved into ethanol (20 mL) with Pd—C (60 mg) and a hydrogen inlet. The mixture was stirred at room temperature until no starting material was detected with TLC or LCMS. Formamidine acetate (0.5 g) was added to the filtrate after the filtration of resulting mixture. The mixture was stirred at 85° C. for 4 hours. Ethyl acetate (40 mL) was added into the resulting mixture, and brine (10 mL×3) was used to wash the organic layer. The organic layer was dried and concentrated. The resulting residue was separated by silica gel column (Ethyl acetate/MeOH) to afford 0.29 g of the title compound. MS (electrospray): 382 (M+1) for C19H20FN7O. 1H NMR (300 MHz, CD3OD) δ ppm 8.45 (s, 1H) 8.35 (s, 1H) 7.75 (d, 1H) 7.50 (s, 1H) 6.70 (d, 1H) 6.00 (s, 1H) 5.10 (m, 1H) 4.50 (m, 1H) 1.55 (d, 3H) 1.35 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486966B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-f064d24ff7de46138640edd8d71b7e56 |
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| Source note | uspto-grants-2013_07 |
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