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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157333Generated: November 2, 2026

Methyl iodide → HCID 68692703, compound

https://huagongshe.com/reaction/1157333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178452277HCID 178452277—
SolventDimethylformamideHCID 6228—
ProductHCID 68692703HCID 68692703—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (0.02 g) was taken in dry DMF (5 ml) and a solution of tert-butyl 4-(5-phenyl-1H-1,2,3-triazol-4-yl)piperazine-1-carboxylate (0.015 g in 5 ml of DMF) was added slowly at 0° C. The reaction mixture was stirred for 30 min at 0° C. and methyl iodide (0.13 g) was added very slowly. The reaction mixture was allowed to stir over night at room temperature. The reaction mixture was quenched with cold water (5 ml) and extracted with ethyl acetate (3×40 ml). Evaporation of solvent under reduced pressure gave crude product, which, was purified by column chromatography using 60-120 silica gel methanol\dichloromethane (1:9) as eluent to afford tert-butyl 4-(2-methyl-5-phenyl-1H-1,2,3-triazol-4-yl)piperazine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807671B2
Source datasetuspto-grants-2010_10
ORD IDord-bd551cd9eb1441499ed53c44ca2d82b3
Source noteuspto-grants-2010_10