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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630464Generated: October 31, 2026

Iodine → HCID 58257834, compound

https://huagongshe.com/reaction/1630464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactanttert-Butyl 4-[6-(trifluoromethyl)pyridazin-3-yl]piperazine-1-carboxylateHCID 53485513—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58257834HCID 5825783482%

Reaction Steps

To a mixture of butyllithium (2.5 M in hexanes) (6.31 ml, 15.79 mmol) in tetrahydrofuran (125 ml) at 0° C., was added 2,2,6,6-tetramethylpiperidine (3.808 ml, 22.56 mmol). The reaction mixture was then stirred at room temperature for 1 h. The mixture was cooled to −78° C. and then a solution of 4-(6-trifluoromethyl-pyridazin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (D9) (2.5 g, 7.52 mmol) in tetrahydrofuran (20 ml) was added. The mixture was stirred for 1 h. at −78° C. before adding a solution of iodine (2.29 g, 9.024 mmol) in tetrahydrofuran (10 ml). The mixture was stirred at −78° C. for 1 h. and then diluted with a 10% solution of acetic acid in tetrahydrofuran. The mixture was then allowed to reach room temperature and then the solvent was evaporated in vacuo. The residue was diluted with dichloromethane and extracted with water. The organic layer was separated, dried (MgSO4), filtered and the solvent evaporated in vacuo. The residue was precipitated from diethyl ether to yield D10 (2.81 g, 82%) as a light yellow solid. C14H18F31N4O2 requires 458; Found 459 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791120B2
Source datasetuspto-grants-2014_07
ORD IDord-b9712f2ca6684eb2ad6a3c48d51db5b7
Source noteuspto-grants-2014_07