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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535453Generated: October 25, 2026

Triethylamine → 3-Amino-6-[(1-methoxy-2-methylindolizin-3yl)carbonyl]quinazoline-2,4(1H,3H)-dione

https://huagongshe.com/reaction/535453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantTriphosgeneHCID 94429—
ReactantMethyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoateHCID 66653263—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-Amino-6-[(1-methoxy-2-methylindolizin-3yl)carbonyl]quinazoline-2,4(1H,3H)-dioneHCID 6665332710.7%

Reaction Steps

0.123 g (0.41 mmol) of triphosgene is added, under an inert atmosphere at ambient temperature, to 0.2 g (0.6 mmol) of methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate in 10 ml of dioxane. After stirring for 10 minutes, 58 μl (1.2 mmol) of hydrazine hydrate and 0.4 ml (3 mmol) of triethylamine are added. The reaction medium is stirred for 3 hours and then hydrolysed with water. The aqueous phase is extracted with ethyl acetate. The organic phase obtained is dried over sodium sulphate, filtered, and then concentrated under reduced pressure. The solid obtained is purified by silica gel column chromatography, elution being carried out with a dichloromethane/methanol (95/5) mixture. 16 mg of a yellow solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859544B2
Source datasetuspto-grants-2014_10
ORD IDord-337cc1c81e154b41b37a65ca2023ad6b
Source noteuspto-grants-2014_10