Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117014Generated: October 26, 2026

Methyl iodide → N-methyl-L-tryptophan

https://huagongshe.com/reaction/2117014

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 (0.284 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439258B2
Source datasetuspto-grants-2008_10
ORD IDord-4d311b15701e4abb81c142600fec6e33
Source noteuspto-grants-2008_10