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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422892Generated: October 30, 2026

Acetic Acid → HCID 67246989, compound

https://huagongshe.com/reaction/1422892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67247636HCID 67247636—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67246989HCID 672469896.4%

Reaction Steps

A solution of piperidin-4-yl-carbamic acid tert-butyl ester (76 mg, 0.38 mmol, 1.0 eq) in 1,2-dichloroethane (1 mL) is added at room temperature to a stirred solution of 6-methoxy-4H-1-oxa-9-aza-phenanthrene-3-one (87 mg, 0.38 mmol, 1.0 eq) in tetrahydrofuran (6 mL), followed by acetic acid (5 μL, 0.08 mmol, 0.2 eq) and the resulting mixture is heated under reflux for 3 hours. The reaction mixture is then cooled down to room temperature before the addition of a solution of sodium cyanoborohydride (48 mg, 0.76 mmol, 2.0 eq) in methanol (1 mL). After 15 hours stirring at room temperature, solvents are evaporated and to give a residue that is purified by preparative HPLC to afford [1-(6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthrene-3-yl)-piperidin-4-yl]-carbamic acid tert-butyl ester as a light yellow solid (10 mg, 6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927541B2
Source datasetuspto-grants-2015_01
ORD IDord-21d9e6ed30874770867bc068f1e178d7
Source noteuspto-grants-2015_01