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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087553Generated: October 29, 2026

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

https://huagongshe.com/reaction/1087553

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 numberUS05036066
Source datasetuspto-grants-1991_07
ORD IDord-cdf3f5e29dc343e8a48659fca20bce2b
Source noteuspto-grants-1991_07