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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712631Generated: November 1, 2026

HCID 117667606, compound → HCID 117667514, compound

https://huagongshe.com/reaction/712631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117667606HCID 117667606—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 117667514HCID 117667514100.2%

Reaction Steps

6-(4-Methoxy-pyridin-3-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester (420 mg, 1.2 mmol) is dissolved in 20% trifluoroacetic acid in DCM (20 mL). The solution is stirred at room temperature for 16 hrs and then the solvent is removed. The residue is dissolved in DCM and saturated aqueous NaHCO3 solution is used to adjust the pH to 9˜10. The organic layer is separated, dried over Na2SO4, filtered and concentrated to give 290 mg of 6-(4-methoxy-pyridin-3-yl)-1,2,3,4-tetrahydro-[1,8]naphthyridine (290 mg crude) which is converted to 38 mg of the titled product according to the procedure of Urea Formation Method I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-f3d48483fdec4ed981e393cb0d7ab834
Source noteuspto-grants-2015_11