Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648542Generated: October 30, 2026

Methyl propiolate → methyl 7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxylate

https://huagongshe.com/reaction/648542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl propiolateHCID 13536—
Reactant3-Hydroxy-2-phenylthiazolo[3,2-a]thieno[2,3-c]pyridinium hydroxideHCID 19020488—
SolventTolueneHCID 1140—
Productmethyl 7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxylateHCID 14666705—

Reaction Steps

(ca) 22.9 g of 3-hydroxy-2-phenylthiazolo[3,2-a]thieno[2,3-c]pyridinium hydroxide (internal salt) and 13.6 ml of methyl propiolate were heated together under argon in 1000 ml of toluene until the starting material was completely taken up. The solvent was removed in vacuo and the residue was stirred in 500 ml of ether/methanol (9:1) for 1 hour. The yellow crystals obtained were removed by filtration under suction. There was obtained methyl 7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxylate of m.p. 153°-154° (dec.). An additional portion of product of m.p. 151°-152° (dec.) can be obtained by chromatography of the filtrate on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735940
Source datasetuspto-grants-1988_04
ORD IDord-3368c8837eae40f2b7afca4248954e01
Source noteuspto-grants-1988_04