HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 3(S)-amino-2-hydroxy-pentanoic acid benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 3-{[(Tert-butoxy)carbonyl]amino}-2-hydroxypentanoic acid | HCID 21962763 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3(S)-amino-2-hydroxy-pentanoic acid benzylamide | HCID 16092596 | — |
Reaction Steps
3-tert-Butoxycarbonylamino-2-hydroxypentanoic acid (300 mg, 1.29 mmol) was combined with EDC (400 mg, 2.1 mmol) and HOBt (400 mg, 2.6 mmol). A solution of benzylamine (0.22 mL) and 4-methylmorpholine (0.5 mL) in dichloromethane (4 mL) was added in one portion. The reaction mixture was stirred at ambient temperature for 2 h. After dilution with ethyl acetate (150 mL), the solution was washed with 1 N aqueous HCl, water, saturated aqueous NaHCO3 solution and brine. The resultant mixture was dried with magnesium sulfate and evaporated under vacuum to yield 3(S)-amino-2-hydroxy-pentanoic acid benzylamide (380 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662849B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-ca77a4aa138d454ab9c9a0c14e3c8604 |
| Source note | uspto-grants-2010_02 |