HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Dimethylaminopyridine → HCID 53860365, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1-{[(Benzyloxy)carbonyl]amino}cyclopropane-1-carboxylic acid | HCID 3589012 | — |
| Reactant | 2,2,5,5-Tetramethylcyclopentanamine | HCID 13247939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53860365 | HCID 53860365 | — |
Reaction Steps
To a stirred solution of N-Cbz-1-aminocyclopropanecarboxylic acid in dry CH2Cl2 containing dicyclohexycarbodiimide and dimethylaminopyridine (DMAP), all at 0° C., is added, via an addition funnel, 2,2,5,5-tetramethyl-1-cyclopentyl amine dissolved in CH2Cl2. After stirring for 48 hours, the mixture is filtered, and the filtrate is washed with 5% HCl (1×50 ml), saturated NaHCO3 (1×50 ml), and water (1×50 ml). The organic layer is separated, dried over MgSO4 and evaporated to yield N-Cbz-1-aminocyclopropanecarboxylic acid 2,2,5,5-tetramethylcyclopentyl amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04678674 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-352b0e81519d4ff5b21c0a7f876cd254 |
| Source note | uspto-grants-1987_07 |