HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-2-Methyl-CBS-oxazaborolidine → HCID 44552953, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-2-Methyl-CBS-oxazaborolidine | HCID 9838490 | — |
| Reactant | HCID 30025967 | HCID 30025967 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Reactant | HCID 178434708 | HCID 178434708 | — |
| Product | HCID 44552953 | HCID 44552953 | — |
Reaction Steps
The procedure given in Example 1 was followed using tert-butyl (3S)-3-[methoxy(methyl)carbamoyl]piperidine-1-carboxylate was used instead of tert-butyl (3R)-3-[methoxy(methyl)carbamoyl]piperidine-1-carboxylate. As a reducing agent, (R)-2-methyl-CBS-oxazaborolidine was used instead of (S)-2-methyl-CBS-oxazaborolidine. And 5-methyl-1H-tetrazole was used as a reactant, instead of 1H-tetrazole, to give (3S)-3-[(S)-(5-methyl-2H-tetrazol-2-yl)(naphthalen-2-yl)methyl]piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513285B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-c22e37b4ae5348a7827525414edc870b |
| Source note | uspto-grants-2013_08 |