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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887080Generated: November 1, 2026

Water → 6-(Piperidin-4-yloxy)-isoquinoline-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1887080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-(5-Iodo-isoquinoline-6-yloxy)-piperidin-1-carboxylic acid tert-butyl esterHCID 57646751—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product6-(Piperidin-4-yloxy)-isoquinoline-5-carboxylic acid ethyl esterHCID 57646961—

Reaction Steps

A solution of 200 mg (0.44 mmol) 4-(5-iodo-isoquinoline-6-yloxy)-piperidin-1-carboxylic acid tert-butyl ester (12), 107 mg (0.88 mmol) of DMAP, 4.7 mg (0.1 eq) of Pd on charcoal (10%), 150 μL (0.88 mmol) of triethyl amine and 58 mg (0.22 mmol) of Mo(CO)6 in 3 mL of ethanol was heated to 135° C. for 1 h in a microwave reactor (CEM Discovery). Then water and ethyl acetate were added and the mixture was filtered through a Celite cartridge. After removal of the solvents the remainder was subjected to preparative HPLC to give the 7.4 mg Boc-protected intermediate. To remove the Boc group the intermediate was treated with 2 mL 5-6 N HCl in isopropanol at room temperature for 2 h. Purification by preparative HPLC gave 2.5 mg of compound 30 as TFA salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501736B2
Source datasetuspto-grants-2013_08
ORD IDord-5691b0130aa941378b40e0bb5db695c1
Source noteuspto-grants-2013_08