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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421972Generated: October 31, 2026

Methanol → tert-Butyl [1-(6-methoxypyridazin-3-yl)piperidin-4-yl]carbamate

https://huagongshe.com/reaction/2421972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodiumHCID 5360545—
Reactant4-(Boc-amino)-1-(6-chloro-3-pyridazinyl)piperidineHCID 37967251—
SolventWaterHCID 962—
Producttert-Butyl [1-(6-methoxypyridazin-3-yl)piperidin-4-yl]carbamateHCID 8662587075%

Reaction Conditions

Temperature120 °C

Reaction Steps

tert-Butyl [1-(6-chloropyridazin-3-yl)piperidin-4-yl]carbamate (0.50 g, 1.60 mmol) was dissolved in dry MeOH (15 ml) and sodium metal (0.073 g, 3.20 mmol) dissolved in MeOH (5 ml) was added. The reaction mixture was heated at in a microwave reactor at 120° C. for 4 h. The mixture was diluted with water (500 ml) and extracted with EtOAc (200 ml). The organic phase was dried (Na2SO4), filtered and evaporated to yield the title compound (0.37 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960380B2
Source datasetuspto-grants-2011_06
ORD IDord-7287a543af424e5b99c45b779645383d
Source noteuspto-grants-2011_06