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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66650707HCID 66650707—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
ProductHCID 42633095HCID 4263309588.4%

Reaction Conditions

Temperature170 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093248B2
Source datasetuspto-grants-2012_01
ORD IDord-8e575756313a490f895e942dd0897966
Source noteuspto-grants-2012_01