HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 66753001, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl pyrrolidine-3-carboxylate hydrochloride | HCID 19261352 | — |
| Reactant | 2-[4-(2-Tert-butylphenyl)piperazin-1-yl]-2-oxoacetic acid | HCID 66750854 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66753001 | HCID 66753001 | 85% |
Reaction Steps
A mixture of 2-[4-(2-tert-butylphenyl)piperazin-1-yl]-2-oxoacetic acid (Example 44, 0.30 g, 1.03 mmol), methyl pyrrolidine-3-carboxylate hydrochloride (0.21 g, 1.2 mmol), triethylamine (215 μL, 1.6 mmol), EDCI (0.19 g, 1.2 mmol) and HOBt (0.19 g, 1.2 mmol) in N,N-dimethylformamide (5 mL) was stirred at room temperature for 2 days. The reaction mixture was poured into saturated NaHCO3 solution and extracted with ethyl acetate. The extract was washed with saturated NaHCO3 solution and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate 85:15 to 35:65) to give the title compound (0.35 g, 85%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-b77a6656980b45b784313dbaa8dd292e |
| Source note | uspto-grants-2014_10 |