HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Aminooxy)propionic acid hydrochloride → 7-(1-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Aminooxy)propionic acid hydrochloride | HCID 20833274 | — |
| Reactant | 7H-indolizino[5,6,7-ij]isoquinolin-7-one | HCID 21552875 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 7-(1-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline | HCID 54435220 | 76.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946019 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-b908cae269cc47d5a67d06e6883292fd |
| Source note | uspto-grants-1976_03 |