Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | HCID 178456057 | HCID 178456057 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 178456056 | HCID 178456056 | — |
Reaction Steps
N6-[(1S)-1-(5-fluoropyridin-2-yl)propyl]-N2-(5-isopropoxy-1H-pyrazol-3-yl)-3-nitropyridine-2,6-diamine (Intermediate 36, 0.45 g) was dissolved into ethanol (20 mL) with Pd—C (150 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 0.12 g desired product. MS (electrospray): 396 (M+1) for C20H22FN7O. 1H NMR (300 MHz, CD3OD) δ ppm 8.40 (s, 1H) 8.30 (s, 1H) 7.70 (d, 1H) 7.50 (m 2H) 6.70 (d, 1H) 6.10 (s, 1H) 5.00 (m, 1H) 4.40 (m, 1H) 2.00 (m, 2H) 1.40 (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-0d4a78b2452f45bf84465d4b819a5577 |
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| Source note | uspto-grants-2013_07 |
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