Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109565Generated: October 25, 2026

1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine → tert-butyl 8-(m-fluorophenyl)-4,5-dihydro-7-oxo-7H-thieno[2,3-a]quinolizine-10-carboxylate

https://huagongshe.com/reaction/1109565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
ReactantHCID 19020416HCID 19020416—
SolventTolueneHCID 1140—
Producttert-butyl 8-(m-fluorophenyl)-4,5-dihydro-7-oxo-7H-thieno[2,3-a]quinolizine-10-carboxylateHCID 19020443—

Reaction Steps

0.96 ml of N,N-dimethylformamide di-t-butyl acetal was added dropwise within 20 minutes to a boiling solution of 0.34 g of 4,5-dihydro-7-oxo-8-(m-fluorophenyl)-7H-thieno[2,3-a]quinolizine-10-carboxylic acid in 5 ml of toluene. The mixture was heated under reflux for an additional 30 minutes, left to stand at room temperature overnight and then washed once with water, twice with saturated aqueous sodium bicarbonate solution and once with saturated aqueous sodium chloride solution. The organic phase was dried over sodium sulfate and evaporated in vacuo. The residue was recrystallized from ethyl acetate and there was obtained tert-butyl 8-(m-fluorophenyl)-4,5-dihydro-7-oxo-7H-thieno[2,3-a ]quinolizine-10-carboxylate of m.p. 135°-137°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05321021
Source datasetuspto-grants-1994_06
ORD IDord-3922151c0c1f482aac5b71db6122eae0
Source noteuspto-grants-1994_06