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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450407Generated: October 29, 2026

Ethanol → HCID 178456056, compound

https://huagongshe.com/reaction/450407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
ReactantFormamidine acetateHCID 160693—
ReactantHCID 178456057HCID 178456057—
CatalystPalladiumHCID 23938—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178456056HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486966B2
Source datasetuspto-grants-2013_07
ORD IDord-0d4a78b2452f45bf84465d4b819a5577
Source noteuspto-grants-2013_07