HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cycloheptanone → N-Cycloheptylglycine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cycloheptanone | HCID 10400 | — |
| Reactant | Glycine methyl ester | HCID 69221 | — |
| Product | N-Cycloheptylglycine | HCID 21197386 | — |
Reaction Steps
N-Cycloheptylglycine was synthesized by reductive amination of cycloheptanone with glycine methyl ester following the procedure described in Gera et al., Immunopharmacology. 33:174–177 (1996). The crude product was converted to the N-Boc derivative (mp, 89–90° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071168B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-4d12ac80a56d479baf43142f1db2788d |
| Source note | uspto-grants-2006_07 |