HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178452375, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Tert-butyl 3-(2-aminoacetamido)azetidine-1-carboxylate | HCID 18699815 | — |
| Reactant | HCID 54574361 | HCID 54574361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178452375 | HCID 178452375 | 101.6% |
Reaction Steps
Under ice cooling, a solution of 4-nitrobenzyl [(4-nitrobenzyloxy)carbonyliminopyrazol-1-ylmethyl]carbamate (1.42 g) in tetrahydrofuran (12 ml) was added to a solution of tert-butyl 3-(aminoacetylamino)-1-azetidinecarboxylate (785 mg) in tetrahydrofuran (13 ml) and the mixture was stirred at room temperature for 3 hours. Ethyl acetate was added to the reaction mixture. The resulting mixture was washed with water, an aqueous solution of potassium hydrogensulfate and saturated saline, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The residue was crystallized from diisopropyl ether, followed by washing, whereby 1.94 g of the title compound were obtained as a colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06090802 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-1e55bd4abc8d44cc8cb873cd09d7b743 |
| Source note | uspto-grants-2000_07 |