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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400328Generated: October 31, 2026

Methyl iodide → 4-(4-bromo-1H-pyrazol-1-yl)-1-methylpiperidine

https://huagongshe.com/reaction/2400328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
Reactant4-(4-Bromo-1H-pyrazol-1-yl)piperidineHCID 52191621—
SolventDimethylformamideHCID 6228—
Product4-(4-bromo-1H-pyrazol-1-yl)-1-methylpiperidineHCID 5959941851%

Reaction Steps

To a solution of 4-(4-bromopyrazol-1-yl)piperidine (480 mg, 2.09 mmol) and triethylamine (0.295 ml, 2.1 mmol) in DMF (4 ml) was added methyl iodide (2.1 ml of a 1.0M solution in DMF, 2.1 mmol) under an inert atmosphere. The reaction was stirred at room temperature overnight, then partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the product (260 mg), which was used without further purification. 1H NMR (400 MHz, CDCl3): 7.47 (1H, s), 7.45 (1H, s), 4.16-4.04 (1H, m), 3.09-2.92 (2H, m), 2.34 (3H, s), 2.30-2.10 (4H, m), 2.10-1.96 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796244B2
Source datasetuspto-grants-2014_08
ORD IDord-2026211a49684f48abf8970d1e018ef3
Source noteuspto-grants-2014_08