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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054746Generated: October 25, 2026

Sodium Chlorite → 6-chloro-5-[4-(1-methylpyrrolidin-3-yl)phenyl]-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1054746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChloriteHCID 23668197—
ReactantSodium Phosphate, Monobasic, DihydrateHCID 23673460—
Reactant6-chloro-5-[4-(1-methylpyrrolidin-3-yl)phenyl]-1H-indole-3-carbaldehydeHCID 86698740—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solventtert-ButanolHCID 6386—
Solvent2-Methyl-2-buteneHCID 10553—
Product6-chloro-5-[4-(1-methylpyrrolidin-3-yl)phenyl]-1H-indole-3-carboxylic acidHCID 866987414.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-chloro-5-[4-(1-methylpyrrolidin-3-yl)phenyl]-1H-indole-3-carbaldehyde (crude, 0.23 g, 0.68 mmol) in acetonitrile (8 mL) and tert-butanol (8 mL) was added 2-methyl-2-butene (8 mL). The reaction mixture was cooled to 0° C. and treated with a solution of sodium chlorite (683 mg, 7.50 mmol) and sodium phosphate monobasic dihydrate (1.59 g, 10.2 mmol) in water (4 mL) dropwise. The reaction mixture was stirred at room temperature for two hours and treated with additional sodium chlorite (911 mg, 10.0 mmol) and sodium phosphate monobasic dihydrate (2.12 g, 13.6 mmol) in H2O (4 mL) and 2-methyl-2-butene (2 mL). The resulting mixture was stirred at room temperature for 16 h. The reaction mixture was evaporated in vacuo and the aqueous residue was extracted with EtOAc (3×30 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified via prep-HPLC to give 6-chloro-5-[4-(1-methylpyrrolidin-3-yl)phenyl]-1H-indole-3-carboxylic acid (10 mg) as a solid. MS (ES+) 354.9 (M+H)+. 1H NMR (400 MHz, CD3OD) δ 8.01 (m, 2 H), 7.59 (s, 1 H), 7.3-7.5 (m, 4 H), 3.40-4.00 (m, 5 H), 3.06 (s, 3 H), 2.1-2.7 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-581b03cb6d2346258a5c9c29ffe97eb4
Source noteuspto-grants-2016_07