Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535443Generated: October 30, 2026

Triethylamine → Methyl {6-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]-2,4-dioxo-1,4-dihydroquinazolin-3(2H)-yl}acetate

https://huagongshe.com/reaction/535443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantGlycine methyl esterHCID 69221—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantTriphosgeneHCID 94429—
ReactantMethyl 2-amino-5-[(1-methoxyindolizin-3-yl)carbonyl]benzoateHCID 66653221—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl {6-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]-2,4-dioxo-1,4-dihydroquinazolin-3(2H)-yl}acetateHCID 6665330586%

Reaction Steps

1.22 g (4.14 mmol) of triphosgene diluted in 15 ml of dioxane are added, under an inert atmosphere at ambient temperature, to 2 g (5.91 mmol) of methyl 2-amino-5-[(1-methoxyindolizin-3-yl)carbonyl]benzoate in 65 ml of dioxane. The reaction medium is stirred for 1 hour at ambient temperature and then 1.48 g (11.82 mmol) of methyl glycinate and 4.12 ml (29.55 mmol) of triethylamine are added. The reaction medium is stirred for 18 hours and then 1.08 g (5.91 mmol) of DBU are added. After stirring for 24 hours, the medium is hydrolysed with water. The aqueous phase is extracted with dichloromethane. The organic phase obtained is washed with water, dried over sodium sulphate, filtered, and then concentrated under reduced pressure. The solid is purified by silica gel column chromatography, elution being carried out with a dichloromethane/methanol (95/5) mixture. The solid obtained is recrystallized, under hot conditions, from methanol. 1.5 g of a yellow solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859544B2
Source datasetuspto-grants-2014_10
ORD IDord-c7fd8677fb4e4edf93f40553eb53d9c5
Source noteuspto-grants-2014_10