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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577785Generated: October 29, 2026

Methyl iodide → HCID 11527262, compound

https://huagongshe.com/reaction/577785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58689767HCID 58689767—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11527262HCID 1152726294.7%

Reaction Steps

To a suspension of sodium hydride (0.023 g, 0.98 mmol) in dry THF (15 mL) at 0° C., in a 25 mL round bottom flask, was added {3-[(3,5-bis-trifluoromethyl-benzylamino)-methyl]-quinolin-2-yl}-cyclopentylmethyl-ethyl-amine (0.25 g, 0.44 mmol), obtained in step (iv) of Example 35. This reaction mixture was stirred for 10 minutes at the same temperature, carbon disulphide (0.112 g, 0.98 mmol) was added dropwise, followed by the addition of methyl iodide (0.208 g, 1.47 mmol). The reaction was allowed to reach RT and stirring was continued for 0.5 h. Water was then added to the reaction, which was then extracted with ethyl acetate. The combined organic layer was washed with brine solution and dried over sodium sulfate. The solvent was evaporated to afford the title compound (0.250 g), yield: 87%, of purity 98.59% (HPLC: Symmetry Shield RP8, [0.01M KH2PO4:CH3CN], 217 nM, Rt 12.221 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040558B2
Source datasetuspto-grants-2015_05
ORD IDord-04e05425a1d5498fa92b29440c125f73
Source noteuspto-grants-2015_05