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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40099Generated: October 26, 2026

2-Methyl-2-butene → 6-Methoxy-2-(methoxycarbonyl)-1-(pyridin-2-ylmethyl)-1H-indole-3-carboxylic Acid

https://huagongshe.com/reaction/40099

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
ReactantMethyl3-Formyl-6-methoxy-1-(pyridin-2-ylmethyl)-1H-indole-2-carboxylateHCID 59762382—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Solvent1,4-DioxaneHCID 31275—
Product6-Methoxy-2-(methoxycarbonyl)-1-(pyridin-2-ylmethyl)-1H-indole-3-carboxylic AcidHCID 59762357—

Reaction Steps

General Procedure K. To a suspension of methyl3-formyl-6-methoxy-1-(pyridin-2-ylmethyl)-1H-indole-2-carboxylate (Compound 91, 1.64 g, 5.07 mmol) in t-BuOH (120 ml) and dioxane (20 ml) was added 2-methyl-2-butene (25 ml) and a solution of NaH2PO4 (7.3 g, 61 mmol) and NaClO2 (80%, 5.7 g, 50.7 mmol) in H2O (100 ml). The reaction was stirred at room temperature for 6 h, extracted with EtOAc (×2). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→100% EtOAc-hexanes) to yield the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524917B2
Source datasetuspto-grants-2013_09
ORD IDord-a90ae63450c6419eacbacb57289ecc8c
Source noteuspto-grants-2013_09