HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417983Generated: October 29, 2026
2-Bromoethyl methyl ether → HCID 42633095, compound
https://huagongshe.com/reaction/417983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 66650707 | HCID 66650707 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 42633095 | HCID 42633095 | 88.4% |
Reaction Steps
2-(piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate (None HCl salt of Example 30; 311 mg, 0.98 mmol) was dissolved in DMF (2 mL). 2-bromoethyl methyl ether (92 μl, 0.98 mmol) and DIPEA (0.3 mL, 1.72 mmol) were added and the reaction mixture was heated at 170° C. for 15 minutes in a Biotage Initiator microwave at high absorption. The reaction mixture was concentrated in vacuo, dissolved in 1 M aq Na2CO3 solution (25 mL) and extracted with DCM (3×25 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by normal phase column chromatography (eluting with DCM, followed by a 200:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-(2-methoxyethyl)-piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate (163 mg, 44%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08093248B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-8e575756313a490f895e942dd0897966 |
|---|
| Source note | uspto-grants-2012_01 |
|---|