HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23322735, compound → HCID 23322734, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23322735 | HCID 23322735 | — |
| Reactant | HCID 23322736 | HCID 23322736 | — |
| Reactant | HCID 86740771 | HCID 86740771 | — |
| Product | HCID 23322734 | HCID 23322734 | — |
| Product | HCID 23322739 | HCID 23322739 | — |
Reaction Steps
Reaction of 3-amino-1-(1-carboxyethyl)- perhydroazonin-2-one (Isomer A, Example 2) with thionyl chloride-ethanol or thionyl chloride-benzyl alcohol followed by concentration and liberation of the free amino ester affords 3-amino-1-(1-ethoxycarbonylethyl)perhydroazonin-2-one and 3-amino-1-(1-benzyloxycarbonylethyl)perhydroazonin-2-one, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587238 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-93546cc8f7c347c9b882ca00c1b36901 |
| Source note | uspto-grants-1986_05 |