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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48915Generated: October 26, 2026

Ethyl 8-(4-Methoxyphenyl)-4-Oxo-4H-Quinolizine-3-Carboxylate → Ethyl 8-(Naphth-1-yl)-4-Oxo-4H-Quinolizine-3-Carboxylate

https://huagongshe.com/reaction/48915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 8-(4-Methoxyphenyl)-4-Oxo-4H-Quinolizine-3-CarboxylateHCID 20634155—
SolventEthyl AcetateHCID 8857—
ProductEthyl 8-(Naphth-1-yl)-4-Oxo-4H-Quinolizine-3-CarboxylateHCID 2063416051%

Reaction Steps

Using the procedure as described in Example 17 (i.e., for compound 22) ethyl 8-(napthy-1-yl)-4-oxo-4H-quinolizine-3-carboxylate (23) was isolated in 51% yield by flash chromatography (ethyl acetate). M.p. 245-247° C. 1H NMR (δ, CDCl3): 1.48 (t, J=7 Hz, 3H), 4.48 (q, J=7 Hz, 2H), 6.73 (d, J=8 Hz, 1H), 7.40 (dd, J=2 Hz, J=8 Hz, 1H), 7.55-7.64 (m, 4H), 7.72 (s, 1H), 7.91 (d, J=8 Hz, 1H), 7.98-8.06 (m, 2H), 8.48 (d, J=8 Hz, 1H), 9.52 (d, J=8 Hz, 1H). MS: m/z 343.1213; required for C22H17NO3: 343.1208.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706528B2
Source datasetuspto-grants-2004_03
ORD IDord-518e2a85d2d24828a7fd7a4f0226eb1f
Source noteuspto-grants-2004_03