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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373892Generated: November 1, 2026

Trimethyl orthoacetate → HCID 21075820, compound

https://huagongshe.com/reaction/1373892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoacetateHCID 15050—
Reactanttert-butyl N'-(3-aminoquinolin-4-yl)hydrazinecarboxylateHCID 21075823—
ReactantEthylacetate methanolHCID 21584119—
CatalystPyridinium chlorideHCID 10176127—
SolventTolueneHCID 1140—
ProductHCID 21075820HCID 2107582084.4%

Reaction Steps

A solution of tert-butyl N′-(3-aminoquinolin-4-yl)hydrazinecarboxylate (11.67 g, 42.5 mmol) in 400 mL of anhydrous toluene was treated with trimethyl orthoacetate (5.96 mL, 46.8 mmol) and pyridine hydrochloride (100 mg) under an atmosphere of N2 and heated to reflux. After stirring for 3 h, the reaction mixture was concentrated under reduced pressure to give a red solid. Chromatography (SiO2, 0–10% MeOH/EtOAc) gave tert-butyl N-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)carbamate (10.7 g) as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163947B2
Source datasetuspto-grants-2007_01
ORD IDord-4698ee159fcf4389a15ee02da25f4d4c
Source noteuspto-grants-2007_01