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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183541Generated: October 30, 2026

Methyl iodide → HCID 10137537, compound

https://huagongshe.com/reaction/2183541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 22474363HCID 22474363—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 10137537HCID 10137537—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of [6-bromo-5-methyl-3-(2,4,6-trimethyl-phenyl)-3H-[1,2,3]triazolo[4,5-b]pyridin-7-yl]-(1-ethyl-propyl)-amine (50 mg, 0.12 mmol) in dry THF )1.5 ml) was added 2.5 M n-BuLi in hexane (0.14 ml) at −78° C. After stirring at −78° C. for 10 min, 0.5 ml of methyl iodide was added at that temperature then allowed to warmed to room temperature and stirred for 15 min for 2 hours. The mixture was quenched with water and extracted with ethyl acetate. The organic layer was washed with brine, dried and concentrated to give 46 mg of brown oil. The residue was purified through silica gel coliumn chromatography using 1:1 chloroform:hexane as eluent to give the title compound as a golden oil. 1H NMR (CDCl3) ä 7.04(s, 2H), 4.35(m, 1H), 3.32(s, 3H), 2.70(s, 3H), 2.38(s, 3H), 1.94(s, 6H), 1.7-2.0(m, 4H), 1.01(t, 6H)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900217B2
Source datasetuspto-grants-2005_05
ORD IDord-8b5081ad7b2d4de7bdec3dbf6a32d151
Source noteuspto-grants-2005_05