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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
ReactantFormamidine acetateHCID 160693—
ReactantHCID 178458651HCID 178458651—
CatalystPalladiumHCID 23938—
SolventSodium chloride; waterHCID 57417360—
ProductN-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-3-(3-propan-2-yloxy-1H-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486966B2
Source datasetuspto-grants-2013_07
ORD IDord-f064d24ff7de46138640edd8d71b7e56
Source noteuspto-grants-2013_07