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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641367Generated: October 30, 2026

Hydrochloric Acid → (-)-5-Amino-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-]pyridin]-2'(1'H)-one

https://huagongshe.com/reaction/641367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantEthylenediamineHCID 3301—
ReactantSodium HydroxideHCID 14798—
Reactant5-amino-1'-((2-(trimethylsilyl)ethoxy)methyl)-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 59166720—
SolventWaterHCID 962—
Product(-)-5-Amino-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-]pyridin]-2'(1'H)-oneHCID 86761077—

Reaction Steps

A solution of (−)-5-amino-1′-{[2-(trimethylsilyl)ethoxy]methyl}-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one from Step B (13.7 g, 35.9 mmol) in methanol (300 mL) was saturated with HCl (g). The mixture was resaturated with HCl (g) every 30 min until the starting material was consumed, and then concentrated in vacuo. The residue was dissolved in MeOH (150 mL) and treated with ethylenediamine (2.4 mL, 35.9 mmol) and 10 N sodium hydroxide (7.2 mL, 72 mmol) to adjust the mixture to pH 10. After 30 min, the mixture was diluted with H2O (400 mL) and extracted with CHCl3 (2×1 L). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The crude material was triturated with MeOH (50 mL) to give the title compound. MS: m/z=252 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696192B2
Source datasetuspto-grants-2010_04
ORD IDord-dcacae630d8743a48e84054418d457db
Source noteuspto-grants-2010_04