HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18417351, compound → HCID 18417358, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18417351 | HCID 18417351 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 18417358 | HCID 18417358 | — |
Reaction Steps
Then, the above 6-azido-5-methoxy-1,3,4-trihydroxy-2-hexanone intermediate is cyclized using reductive amination conditions with hydrogen and a catalyst for producing the 2-hydroxymethyl-3,4-dihydroxy-5-methoxypiperidine with the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462193B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-c2307affc9574a9c9f952ebe4afc6423 |
| Source note | uspto-grants-2002_10 |