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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018270Generated: October 25, 2026

Methyl iodide → N-methyl-L-tryptophan

https://huagongshe.com/reaction/1018270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantOxitriptanHCID 439280—
SolventDimethylformamideHCID 6228—
ProductN-methyl-L-tryptophanHCID 160511—

Reaction Steps

The protected tryptophan derivative from above (0.573 g, 1.00 mmol) was dissolved in DMF (3 mL) and the solution cooled in ice. Sodium hydride (60% oil dispersion, 0.048 g, 1.2 mmol) was added and the mixture stirred for 30 min. Iodomethane (0.093 mL, 1.5 mmol) was added and stirring continued for an additional hour. The reaction was then quenched with 10% citric acid (2 mL) and water (25 mL), and extracted with Et2O (100 mL). The extract was dried (MgSO4) and concentrated, and the residue purified by flash chromatography (20-30% EtOAc/hexane as eluent) to give the desired N-methyltryptophan derivative (0.284g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479508B1
Source datasetuspto-grants-2002_11
ORD IDord-f490b21ab9e64a7581a4f9d22a7a0000
Source noteuspto-grants-2002_11