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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338443Generated: October 27, 2026

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

https://huagongshe.com/reaction/338443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
Reactant5-[4-(azetidin-3-yl)phenyl]-6-chloro-1H-indole-3-carbaldehydeHCID 86698773—
Solvent2-Methyl-2-butene t-butanol waterHCID 23084028—
Product5-[4-(azetidin-3-yl)phenyl]-6-chloro-1H-indole-3-carboxylic acidHCID 8669877410.2%

Reaction Steps

To 5-[4-(azetidin-3-yl)phenyl]-6-chloro-1H-indole-3-carbaldehyde (94 mg, 0.30 mmol) in 2-methyl-2-butene/t-BuOH/H2O (v/v/v=1/1/1, 4 mL) was added sodium dihydrogen phosphate (364 mg, 3.04 mmol) and sodium chlorite (274 mg, 3.04 mmol) at room temperature. The resulting mixture was stirred at room temperature for 24 hours. To the reaction mixture was added sodium sulfite (383 mg, 3.04 mmol), then concentrated in vacuo and purified via reverse phase HPLC to give the title compound (10 mg, 10% yield). 1H NMR (400 MHz, CD3OD) δ 8.03-80.4 (d, 2H), 7.62 (s, 1H), 7.48-7.52 (m, 4H), 4.44-4.48 (m, 2H), 4.32-4.34 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-f9d2e966535044ffb724f3d65b9250c3
Source noteuspto-grants-2014_11