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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275544Generated: October 31, 2026

Lithium Hydroxide → (1R)-1'-{[1-(6-pyrrolidin-1-ylpyridin-3-yl)cyclopropyl]carbonyl}-3H-spiro[furo[3,4-c]pyridine-1,3'-pyrrolidin]-3-one

https://huagongshe.com/reaction/2275544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantEthyl 1-(6-pyrrolidin-1-ylpyridin-3-yl)cyclopropanecarboxylateHCID 66661814—
Reactant3H-spiro[furo[3,4-c]pyridine-1,3'-pyrrolidin]-3-one dihydrochlorideHCID 66662175—
SolventMethanolHCID 887—
Product(1R)-1'-{[1-(6-pyrrolidin-1-ylpyridin-3-yl)cyclopropyl]carbonyl}-3H-spiro[furo[3,4-c]pyridine-1,3'-pyrrolidin]-3-oneHCID 66662063—

Reaction Steps

The above material of ethyl 1-(6-pyrrolidin-1-ylpyridin-3-yl)cyclopropanecarboxylate was treated with LiOH in methanol to afford the corresponding acid, which was then coupled with 3H-spiro[furo[3,4-c]pyridine-1,3′-pyrrolidin]-3-one dihydrochloride using procedures analogous to those for example 96 to afford (1R)-1′-{[1-(6-pyrrolidin-1-ylpyridin-3-yl)cyclopropyl]carbonyl}-3H-spiro[furo[3,4-c]pyridine-1,3′-pyrrolidin]-3-one. MS (ESI): (M+H)+=405.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126927B2
Source datasetuspto-grants-2015_09
ORD IDord-cee47f17daea4a3f903963580df65d30
Source noteuspto-grants-2015_09