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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42447Generated: October 27, 2026

Isopropyl iodide → Methyl 1-(1-methylethyl)-7-(methyloxy)-1H-indole-4-carboxylate

https://huagongshe.com/reaction/42447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 7-methoxy-1H-indole-4-carboxylateHCID 11020003—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-(1-methylethyl)-7-(methyloxy)-1H-indole-4-carboxylateHCID 6746865594.8%

Reaction Steps

To a cooled (ice/water bath) solution of methyl 7-(methyloxy)-1H-indole-4-carboxylate (350 mg, 1.706 mmol) in DMF (20 mL) was added sodium hydride (56.0 mg, 2.217 mmol). After 10 minutes added 2-iodopropane (0.188 mL, 1.876 mmol). The reaction was stirred at RT for 1 h, followed by heating at 50° C. for 2 h. The reaction was then cooled in an ice water bath and more sodium hydride (56.0 mg, 2.217 mmol) and 2-iodopropane (0.188 mL, 1.876 mmol) were added. The reaction was heated at 50° C. for 3 h, at which time it was concentrated. The residue was dissolved in DCM and washed with water and brine, dried over MgSO4, filtered and concentrated to give 400 mg of the title compound. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.49 (d, 6H), 3.95 (s, 3H), 4.01 (s, 3H), 5.46 (dt, J=13.39, 6.69 Hz, 1H), 6.66 (d, J=8.34 Hz, 1H), 7.15 (d, J=3.03 Hz, 1H), 7.34 (d, J=3.28 Hz, 1H), 7.87 (d, J=8.34 Hz, 1H). MS (ES) [M+H]+ 248.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536179B2
Source datasetuspto-grants-2013_09
ORD IDord-080dd5acd25040359a48dfeb0ac2c5d2
Source noteuspto-grants-2013_09