HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2-[4-(2-tert-butylphenyl)piperazin-1-yl]-N-(2-hydroxy-2-methylpropyl)-2-oxoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2-Propanol, 1-amino-2-methyl- | HCID 95102 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[4-(2-Tert-butylphenyl)piperazin-1-yl]-2-oxoacetic acid | HCID 66750854 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[4-(2-tert-butylphenyl)piperazin-1-yl]-N-(2-hydroxy-2-methylpropyl)-2-oxoacetamide | HCID 66751354 | 102.1% |
Reaction Steps
A solution of [4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetic acid (Example 44, 0.300 g, 1.03 mmol), 1-amino-2-methylpropan-2-ol (0.111 g, 1.24 mmol), EDCI (0.238 g, 1.24 mmol) and HOBt (0.168 g, 1.24 mmol) in acetonitrile (5 mL) was stirred at room temperature for 16 h. The reaction mixture was poured into saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layer was washed with saturated sodium hydrogen carbonate solution and brine, dried over MgSO4, and the solvent was evaporated under reduced pressure to provide 2-[4-(2-tert-butylphenyl)piperazin-1-yl]-N-(2-hydroxy-2-methylpropyl)-2-oxoacetamide (0.380 g, quant) as a white amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-663376e80fba43bbac9de3ee4e8c9a3b |
| Source note | uspto-grants-2014_10 |