HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-((Tert-butoxy)carbonyl)-3,3-dimethylpyrrolidine-2-carboxylic acid → 1-(tert-butoxycarbonyl)-3,3-dimethylprolyl-N-[5-chloro-2-(1H-tetraazol-yl)-benzyl]-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-((Tert-butoxy)carbonyl)-3,3-dimethylpyrrolidine-2-carboxylic acid | HCID 4059597 | — |
| Reactant | N-[5-chloro-2-(1H-tetraazol-1-yl)benzyl]-L-prolinamide | HCID 69655818 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-(tert-butoxycarbonyl)-3,3-dimethylprolyl-N-[5-chloro-2-(1H-tetraazol-yl)-benzyl]-L-prolinamide | HCID 69656113 | — |
Reaction Steps
The title compound was prepared as a mixture of diastereomers from 1-(tert-butoxycarbonyl)-3,3-dimethyl-dl-proline (61 mg, 0.25 mmol) and N-[5-chloro-2-(1H-tetrazol-1-yl)benzyl]-L-prolinamide (Example 26, Step B, 95 mg, 0.25 mmol) essentially according to the EDC coupling procedure described in Example 39, Step D. The diastereomeric products were separated by reverse phase HPLC and were carried on directly to deprotection.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07144899B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-4694cd1689aa47b68449eee806b6c3ae |
| Source note | uspto-grants-2006_12 |