HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Aminooxy)propanoic acid hydrochloride → 7-(2-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Aminooxy)propanoic acid hydrochloride | HCID 12604317 | — |
| 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-(2-carboxyethoxyimino)-7H-indolizino[5,6,7-ij]isoquinoline | HCID 54288921 | 75.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946019 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-8afcfd7615674657a28a1b63174ef5fb |
| Source note | uspto-grants-1976_03 |