HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminooxyacetic acid hemihydrochloride → 7-carboxymethoxyimino-7H-indolizino[5,6,7-ij]isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminooxyacetic acid hemihydrochloride | HCID 2723609 | — |
| Reactant | Isoquinoline-7-one | HCID 67245344 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 7-carboxymethoxyimino-7H-indolizino[5,6,7-ij]isoquinoline | HCID 53703446 | 111.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946019 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-cc3828a225d4456ea65f0881f0978485 |
| Source note | uspto-grants-1976_03 |