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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267992Generated: October 28, 2026

3-(Aminooxy)propanoic acid hydrochloride → 7-(2-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline

https://huagongshe.com/reaction/267992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Aminooxy)propanoic acid hydrochlorideHCID 12604317—
Reactant7H-indolizino[5,6,7-ij]isoquinolin-7-oneHCID 21552875—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product7-(2-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinolineHCID 5428892175.2%

Reaction Steps

A solution of 3-aminooxypropionic acid hydrochloride (12 g.) in water (36 cc.) is added to a stirred boiling solution of 7H-indolizino[5,6,7-ij]isoquinolin-7-one (12 g.) in ethanol (360 cc.) and pyridine (6.64 g.). Boiling is maintained for 3 hours 10 minutes. After cooling, the yellow crystals obtained are filtered off and then washed with 90% ethanol, with absolute ethanol and finally with diethyl ether. After drying, 7-(2-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline (12.59 g.), melting at 250° C. with decomposition, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03946019
Source datasetuspto-grants-1976_03
ORD IDord-8afcfd7615674657a28a1b63174ef5fb
Source noteuspto-grants-1976_03