HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 45274820, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(3,4-Dimethoxybenzyl)-2-methylpiperazine | HCID 20363969 | — |
| Reactant | 2-(2-Oxo-3,3-diphenylpyrrolidin-1-yl)acetic acid | HCID 67359013 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 45274820 | HCID 45274820 | — |
Reaction Steps
To 2-(3,4-dimethoxybenzyl)-2-methylpiperazine (0.052 g, 0.208 mmol; German Patent No. DE2438725), 2-(2-oxo-3,3-diphenylpyrrolidin-1-yl)acetic acid (0.061 g, 0.208 mmol; Example 1C) and 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (0.079 g, 0.208 mmol) in dichloromethane (0.5 mL) was added diisopropylethylamine (0.054 mL, 0.312 mmol) and the reaction stirred overnight. The reaction was loaded onto silica gel and the product eluted using a gradient of 0.5% methanol/dichloromethane to 5% methanol/dichloromethane containing 7 N NH3 over 30 minutes to provide the title compound. MS (ESI+) m/z 528.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044069B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-b4dac419b4774c66952de043d43c31de |
| Source note | uspto-grants-2011_10 |