HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 131728271, compound → HCID 131728273, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 131728271 | HCID 131728271 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131728273 | HCID 131728273 | 100% |
Reaction Steps
3.3 g (9.9 mmol) of N-benzyl-N-methyl-L-alanyl-D-lactic acid piperidide are hydrogenated in 100 ml of ethanol in the presence of 0.35 g of Pd(OH)2-carbon [20% Pd content] until absorption of hydrogen is complete (about 4 hours). After filtering off the catalyst, the entire reaction solution is concentrated in vacuo. 2.4 g (100% of theory) of N-methyl-L-alanyl-D-lactic acid piperidide are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772190B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-0df5ecb95e2a46e6922897df34328178 |
| Source note | uspto-grants-2010_08 |