Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279293Generated: October 30, 2026

Triphenylphosphine → HCID 178487968, compound

https://huagongshe.com/reaction/2279293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant6-Methoxy-[1,5]naphthyridin-3-olHCID 136379414—
ReactantHCID 178453925HCID 178453925—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178487968HCID 17848796854.3%

Reaction Conditions

Temperature30 °C

Reaction Steps

Diethyl azodicarboxylate (3.96 g, 22.72 mmol, 3.0 eq) is added at room temperature to a stirred solution of [trans-4-(2-hydroxy-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (1.84 g, 7.57 mmol, 1.0 eq), 6-methoxy-[1,5]naphthyridin-3-ol (1.80 g, 10.22 mmol, 1.35 eq) and triphenylphosphine (5.96 g, 22.72 mmol, 3.0 eq) in tetrahydrofuran (70 mL). After 14 hours stirring at 30° C., tetrahydrofuran is evaporated and the resulting crude product is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 6:1, v/v) to afford {trans-4-[2-(6-methoxy-[1,5]naphthyridin-3-yloxy)-ethyl]-cyclohexyl}-carbamic acid tert-butyl ester as an off-white solid (1.65 g, 53.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133219B2
Source datasetuspto-grants-2015_09
ORD IDord-b4697c5801a64265a3d3435b39b379eb
Source noteuspto-grants-2015_09