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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267988Generated: November 2, 2026

2-(Aminooxy)propionic acid hydrochloride → 7-(1-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline

https://huagongshe.com/reaction/267988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Aminooxy)propionic acid hydrochlorideHCID 20833274—
Reactant7H-indolizino[5,6,7-ij]isoquinolin-7-oneHCID 21552875—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product7-(1-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinolineHCID 5443522076.4%

Reaction Steps

A solution of 2-aminooxypropionic acid hydrochloride (15.0 g.) in water (37.5 cc.) is added to a stirred boiling solution of 7H-indolizino[5,6,7-ij]isoquinolin- 7-one (15.0 g.) in ethanol (375 cc.) and pyridine (8.14 g.). Boiling is maintained for 2 hours 30 minutes. After cooling, the orange crystals are filtered off, washed with 90% ethanol, then with absolute ethanol and finally with diethyl ether. After drying, 7-(1-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline (16.0 g.), melting at 225° C. with decomposition, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03946019
Source datasetuspto-grants-1976_03
ORD IDord-b908cae269cc47d5a67d06e6883292fd
Source noteuspto-grants-1976_03