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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348962Generated: October 25, 2026

Butyl iodide → 1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acid

https://huagongshe.com/reaction/348962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium HydroxideHCID 14797—
Reactantmethyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylateHCID 21086207—
SolventDimethylformamideHCID 6228—
Product1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acidHCID 21085174—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of methyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylate (0.437 g) in DMF(15 mL) was added potassium hydroxide (0.087 g) and iodobutane (0.34 mL). The mixture was heated to 70° C. for 6 h. then stirred at room temperature for 72 h. The mixture was partitioned between water and ethyl acetate, the layers were separated and the organic layer washed three times with water. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was dissolved in methanol (5 mL) to which was added 1N NaOH (2 mL) and the mixture heated to 50° C. for 1 h. The mixture was cooled to room temperature and poured into water and washed with ether. The aqueous layer was acidified to pH 4 with 1N HCl and the product extracted into ethyl acetate which was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to give 0.377 g of the title compound: 1H NMR (CDCl3) δ 0.973, 1.38, 1.87, 3.01, 3.45, 4.21, 6.71, 7.36, 7.82, 8.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-385f4bb1a3254dd98da25b54207bc336
Source noteuspto-grants-2007_02