HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → cyclopentyl(2S)-2-[(tert-butoxycarbonyl)amino]pent-4-ynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Cyclopentanol | HCID 7298 | — |
| Reactant | (2S)-2-{[(tert-butoxy)carbonyl]amino}pent-4-ynoic acid | HCID 2734488 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | cyclopentyl(2S)-2-[(tert-butoxycarbonyl)amino]pent-4-ynoate | HCID 59243606 | 83% |
Reaction Steps
To a solution of Boc-L-propargyl glycine (5 g, 23.45 mmol) in DCM (100 ml) was added cyclopentanol (3.03 g, 35.2 mmol), EDC (4.93 g, 25.8 mmol) and DMAP (0.286 g, 2.345 mmol). The mixture was stirred overnight at RT. The solvent was removed under reduced pressure and the residue was subjected to column chromatography eluting with 7 to 12% EtOAc in hexanes. Yield=5.5 g, 19.55 mmol, 83% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106091B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-08b3bbf783e44372bbe0a66aadeaf06a |
| Source note | uspto-grants-2012_01 |