Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075586Generated: October 31, 2026

Piperidine → HCID 50882150, compound

https://huagongshe.com/reaction/2075586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11342430HCID 11342430—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 50882150HCID 5088215069.5%

Reaction Steps

N-[5-tert-Butyl-2-methoxy-3-(piperidine-1-carbonyl)-phenyl]-2-[4-(2-morpholin-4-yl-ethoxy)-naphthalen-1-yl]-2-oxo-acetamide (31) 26 mg (0.049 mmol) of the compound obtained above was converted to the acid chloride by reaction with oxalyl chloride (54 μl, 0.5 mmol) in 0.5 mL DCM in the presence of a catalytic amount of DMF (rt, 2 h). After removal of the solvent, the crude acid chloride was dissolved in 1 mL DCM. DIEA (0.2 mmol) was added, followed by the addition of piperidine (0.1 mmol). The resulting mixture was stirred at rt overnight. Aqueous work-up and purification by LC-MS resulted in 7.6 mg pure product. Calculated mass=602. Observed mass=602

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919617B2
Source datasetuspto-grants-2011_04
ORD IDord-8c347d71895a4997a398798dae00d64c
Source noteuspto-grants-2011_04