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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363585Generated: October 29, 2026

Ammonium formate → HCID 57515430, compound

https://huagongshe.com/reaction/1363585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 57515434HCID 57515434—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 57515430HCID 5751543064%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 1-{[4-(dibenzylamino)-6,7-dimethyl-2-propyl-1H-imidazo[4,5-c]pyridin-1-yl]methyl}cyclohexanol (1.50 g, 3.02 mmol), ammonium formate (2.84 g, 45.0 mmol), and 10% palladium on carbon (1.50 g) in methanol (60 mL) and ethanol (120 mL) was heated at 85° C. for 2 h. More ammonium formate (1.00 g) was added and heating was continued of 3 h, then the reaction mixture was stirred overnight at rt. The mixture was filtered through CELITE filter agent and the filtrate was concentrated in vacuo. The crude product was purified using HPFC (gradient elution with 10-40% CMA/chloroform). The appropriate fractions were concentrated and the resulting solid was triturated with acetonitrile. A solid was isolated by filtration and dried at 100° C. under vacuum to provide 1-[(4-amino-6,7-dimethyl-2-propyl-1H-imidazo[4,5-c]pyridin-1-yl)methyl]cyclohexanol as a white powder (0.61 g, 64%), mp 214.0-216.0° C. Anal. Calcd for C18H29N4O C, 68.32; H, 8.92; N, 17.71. Found: C, 68.06; H, 8.65; N, 17.45

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884207B2
Source datasetuspto-grants-2011_02
ORD IDord-e3fcdb105a2744aa85dc7e9ee232aa01
Source noteuspto-grants-2011_02