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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594009Generated: November 2, 2026

Hydrochloric Acid → 1-[5-(3-Methyl-[1,2,4]-oxadiazol-5-yl)thiazol-2-yl]piperazine

https://huagongshe.com/reaction/1594009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl 4-[5-(3-methyl-[1,2,4]-oxadiazol-5-yl)-thiazol-2-yl]piperazine-1-carboxylateHCID 69423493—
Solvent1,2-DichloroethaneHCID 11—
Product1-[5-(3-Methyl-[1,2,4]-oxadiazol-5-yl)thiazol-2-yl]piperazineHCID 6852813996.8%

Reaction Steps

A satd ethanolic HCl soln (4 ml) was added to a solution of 220 mg (0.63 mmol) of tert-butyl 4-[5-(3-methyl-[1,2,4]-oxadiazol-5-yl)thiazol-2-yl]-piperazine-1-carboxylate [Precursor BBB62] in DCE (10 ml). After stirring at RT 5 min, the reaction solution was concentrated in vacuo. The residue was taken up in DCM and washed successively with a 1% strength aq. NaOH soln and water. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. 152 mg (0.61 mmol, 96%) of 1-[5-(3-methyl-[1,2,4]-oxadiazol-5-yl)thiazol-2-yl]piperazine were obtained here.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300939B2
Source datasetuspto-grants-2007_11
ORD IDord-1532c660678f43f788234b1dcb848902
Source noteuspto-grants-2007_11