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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490289Generated: October 29, 2026

Ammonium formate → 1-(3-Methyl-isoquinolin-5-yl)-3-pyrrolidin-3-yl urea

https://huagongshe.com/reaction/490289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-(1-Benzyl-pyrrolidin-3-yl)-3-(3-methyl-isoquinolin-5-yl)ureaHCID 10428622—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product1-(3-Methyl-isoquinolin-5-yl)-3-pyrrolidin-3-yl ureaHCID 6885574569.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (D3) (2.30 g, 6.40 mmol), ammonium formate (2.02 g, 32.10 mmol) and 10% palladium on carbon (1 g) in methanol (100 mL) was heated at 70° C. for 3 h, then cooled to 25° C. and filtered through Celite. Evaporation in vacuo gave an oil which was suspended in dichloromethane and washed with saturated sodium carbonate solution. The organic layer was removed, dried (Na2SO4), and the solvents evaporated in vacuo to give the title compound as a yellow oil (1.2 g). 1H NMR (CDCl3) δ: 2.05-2.20 (2H, m), 2.68 (3H, s), 2.85-2.95 (2H, m), 3.00-3.15 (2H, m), 4.35-4.45 (1H, m), 5.85-5.90 (1H, m), 7.40-7.50 (2H, m), 7.62 (1H, s), 7.72 (1H, d, J=8.2 Hz), 7.91 (1H, d, J=7.6 Hz), 9.14 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528150B2
Source datasetuspto-grants-2009_05
ORD IDord-2e7d56c0bcf74146a804d5c5f54f7776
Source noteuspto-grants-2009_05