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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915341Generated: October 30, 2026

Methyl iodide → ethyl 1-methyl-5-nitro-3-phenyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/915341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactantethyl 5-nitro-3-phenyl-1H-indole-2-carboxylateHCID 741309—
SolventDimethylformamideHCID 6228—
Productethyl 1-methyl-5-nitro-3-phenyl-1H-indole-2-carboxylateHCID 69231753—

Reaction Steps

A solution of ethyl 5-nitro-3-phenyl-1H-indole-2-carboxylate (1.0 g, 3.23 mmol) and iodomethane (2.5 mL, 40.2 mmol) in DMF (25 mL) was treated with Cs2CO3 (3.26 g, 10 mmol) and stirred for 16 h. The reaction was quenched by addition of water and the solid was collected and dried to yield ethyl 1-methyl-5-nitro-3-phenyl-1H-indole-2-carboxylate (I13064-48) as a yellowish solid (1.1 g, 100%): 1H NMR (DMSO-d6) δ 1.03 (t, J=7.0 Hz, 3 H), 4.09 (s, 3 H), 4.18 (q, J=7.0 Hz, 2 H), 7.40-7.55 (m, 5 H), 7.90 (d, J=9.2 Hz, 1 H), 8.23 (dd, J=9.2, 2.3 Hz, 1H), 8.32 (d, J=2.3 Hz, 1 H); MS (EI) m/z 325.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265148B2
Source datasetuspto-grants-2007_09
ORD IDord-6a8c455eba574f72baeaa63526bd216b
Source noteuspto-grants-2007_09