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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267987Generated: October 31, 2026

Aminooxyacetic acid hemihydrochloride → 7-carboxymethoxyimino-7H-indolizino[5,6,7-ij]isoquinoline

https://huagongshe.com/reaction/267987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminooxyacetic acid hemihydrochlorideHCID 2723609—
ReactantIsoquinoline-7-oneHCID 67245344—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product7-carboxymethoxyimino-7H-indolizino[5,6,7-ij]isoquinolineHCID 53703446111.5%

Reaction Steps

A solution of aminooxyacetic acid hemihydrochloride (60.0 g.) in water (180 cc.) is added to a stirred boiling solution of 7H-indolizino 5,6,7-ij]isoquinolin-7-one (60.0 g.) in ethanol (1,800 cc.) and pyridine (27.3 cc.). Boiling is maintained for 2 hours 30 minutes. After cooling, the yellow crystals obtained are filtered off, washed with 90% ethanol, then with absolute ethanol and finally with diethyl ether. After drying, 7-carboxymethoxyimino-7H-indolizino[5,6,7-ij]isoquinoline (67.6 g.), melting at 212° C. with decomposition, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03946019
Source datasetuspto-grants-1976_03
ORD IDord-cc3828a225d4456ea65f0881f0978485
Source noteuspto-grants-1976_03