HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178471825, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 131734633 | HCID 131734633 | — |
| Reactant | HCID 178464106 | HCID 178464106 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 178471825 | HCID 178471825 | 121.8% |
Reaction Steps
22 g of H-Arg(diAc)-OCH2CH2N(CH2CH3)2 was dissolved in 300 ml of 5% NaHCO3. 24 g of Boc-Asp(OEt)-Pro-OSu in 150 ml of acetone was added into the reaction mixture. The mixture was stirred for 5 h at RT. 500 ml of ethyl acetate was added into the mixture. The ethyl acetate solution was washed with water (3×100 ml). The organic solution was dried over sodium sulfate. The solution was evaporated to dryness. The residue was dissolved in 250 ml of dichloromethylene. 200 ml of trifluoroacetic acid was added into the mixture and the mixture was stirred for 30 min. The mixture was evaporated to dryness to yield 32 g of H-Asp(OEt)-Pro-Arg(diAc)*OCH2CH2N(CH2CH3)2.2TFA.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09248109B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-90eae7552fdf4892badd0f832a68a13b |
| Source note | uspto-grants-2016_02 |