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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802992Generated: November 1, 2026

Methyl iodide → (R)-3-[8-(3,4-difluoro-benzyloxy)-octanoylamino]-4-trimethylammonio-butyrate

https://huagongshe.com/reaction/1802992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium BicarbonateHCID 516893—
Reactant(R)-3-[8-(3,4-difluoro-benzyloxy)-octanoylamino]-4-dimethylamino-butyric acidHCID 46223510—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product(R)-3-[8-(3,4-difluoro-benzyloxy)-octanoylamino]-4-trimethylammonio-butyrateHCID 44465161—

Reaction Steps

Potassium hydrogencarbonate (24 mg, 0.24 mmol) and iodomethane (106 mg, 0.74 mmol) were added to a solution of (R)-3-[8-(3,4-difluoro-benzyloxy)-octanoylamino]-4-dimethylamino-butyric acid (77 mg, 0.19 mmol) in methanol (2.5 mL). The reaction mixture was stirred at room temperature for 16 h, then diluted with chloroform (5 mL). Insoluble material was removed by filtration to afford (R)-3-[8-(3,4-difluoro-benzyloxy)-octanoylamino]-4-trimethylammonio-butyrate as a light yellow solid, m/e=429.3 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349893B2
Source datasetuspto-grants-2013_01
ORD IDord-7d5cae9ff22a48c396ff3364c61428b5
Source noteuspto-grants-2013_01