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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511795Generated: November 4, 2026

Sulfuric acid magnesium salt (1:1) → HCID 66954028, compound

https://huagongshe.com/reaction/1511795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(-)-EpichlorohydrinHCID 2734062—
SolventMethanolHCID 887—
ProductHCID 66954028HCID 66954028—

Reaction Conditions

Temperature35 °C

Reaction Steps

A solution of piperazine-1-carboxylic acid tert-butyl ester (commercial; 1.40 g, 7.6 mmol) in dry MeOH (25 mL) was treated with MgSO4 (1.9 g). (R)-Epichlorohydrin (1.47 mL, 18.9 mmol) was added dropwise and the mixture was heated at 35° C. for 2 h and was then stirred at rt overnight. The mixture was filtered over Celite and concentrated under reduced pressure. The residue was taken up in DCM and washed with water. The org. phase was dried over MgSO4 and concentrated under reduced pressure to afford the crude 4-((R)-3-chloro-2-hydroxy-propyl)-piperazine-1-carboxylic acid tert-butyl ester. To a solution of the above intermediate chlorohydrin (2.10 g, 7.53 mmol) and (2,3-dihydro-benzo[1,4]dioxin-6-yl)-carbamic acid benzyl ester (2.15 g, 1 eq, prepared according to WO2007107965) in DMF (30 mL) was added LiOtBu (10.3 mL, 2.2M in THF) at rt. The mixture was stirred at rt over night and subsequently at 50° C. for 5 h. The mixture was partitioned between EA and 0.5M HCl. The aq. phase was basified (NH4OH) and extracted with EA. The org. layer was dried over MgSO4 and concentrated under reduced pressure to afford the title compound as a colorless solid (1.15 g, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217029B2
Source datasetuspto-grants-2012_07
ORD IDord-e2754ef9da454c8091fdc2961f633909
Source noteuspto-grants-2012_07