HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23322736, compound → HCID 23322738, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23322736 | HCID 23322736 | — |
| Reactant | HCID 23322743 | HCID 23322743 | — |
| Reactant | HCID 86740771 | HCID 86740771 | — |
| Product | HCID 23322738 | HCID 23322738 | — |
| Product | HCID 23322750 | HCID 23322750 | — |
Reaction Steps
Reaction of 3-amino-1-t-butylcarbonylmethyl- perhydroazonin-2-one (Example 1) with thionyl chloride-ethanol or thionyl chloride-benzyl alcohol followed by concentration and liberation of the free amino ester affords 3-amino-1-ethoxycarbonylmethylperhydroazonin-2-one and 3-amino-1-benzyloxycarbonylmethylperhydroazonin-2-one, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587238 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-33453ef06dcd4424ab76038a59215b15 |
| Source note | uspto-grants-1986_05 |