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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13701Generated: October 26, 2026

Methyl iodide → 3-(1-Ethyl-5-fluoro-indan-1-yl)-1-methyl-7-nitro-1H-indole

https://huagongshe.com/reaction/13701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium MethoxideHCID 10942334—
Reactant3-(1-Ethyl-5-fluoro-indan-1-yl)-7-nitro-1H-indoleHCID 11609506—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3-(1-Ethyl-5-fluoro-indan-1-yl)-1-methyl-7-nitro-1H-indoleHCID 1157363095.6%

Reaction Steps

Combine 3-(1-ethyl-5-fluoro-indan-1-yl)-7-nitro-1H-indole (0.33 g, 1.02 mmol), sodium methoxide (110 mg, 2.04 mmol), and iodomethane (0.10 ml, 1.53 mmol) in dimethylformamide (5 ml) and stir at room temperature under nitrogen overnight. Dilute with ether, wash with water (2×), dry over sodium sulfate, filter, and concentrate to obtain the title compound as a yellow amorphous solid (0.33 g, 94%). LC-MS m/z 339.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728150B2
Source datasetuspto-grants-2010_06
ORD IDord-becbe1a517f8420a8d9ed13574665c82
Source noteuspto-grants-2010_06