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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340158Generated: November 2, 2026

Methanol → Methyl (2R)-2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridine]-5-carboxylate

https://huagongshe.com/reaction/340158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium AcetateHCID 517045—
Reactant(2R)-5-iodo-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 58118662—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductMethyl (2R)-2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridine]-5-carboxylateHCID 86695345—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of (2R)-5-iodo-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one (100.0 g, 276 mmol), sodium acetate (45.3 g, 552 mmol) and Pd(dppf)Cl2—CH2Cl2 (11.3 g, 13.8 mmol) in a mixture of MeOH (1 L) and toluene (30 mL) was pressurized to 120 psi of CO at 23° C. and then heated at 80° C. for 12 h with stirring. The reaction mixture was diluted with water (1 L), and the precipitate collected by filtration, washed with water, and dried under nitrogen atmosphere to give the title compound, which was used without further purification. MS: m/z=295.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895572B2
Source datasetuspto-grants-2014_11
ORD IDord-79372ebc255546d59b2affe65a04fc39
Source noteuspto-grants-2014_11