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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391190Generated: October 29, 2026

4-{3-[2-Fluoro-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenylamino]-propyl}-tetrahydro-pyran-4-carboxylic acid methyl ester → 2-[2-Fluoro-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenyl]-9-oxa-2-aza-spiro[5.5]undecan-1-one

https://huagongshe.com/reaction/391190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-{3-[2-Fluoro-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenylamino]-propyl}-tetrahydro-pyran-4-carboxylic acid methyl esterHCID 58468077—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-[2-Fluoro-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenyl]-9-oxa-2-aza-spiro[5.5]undecan-1-oneHCID 46223710—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-{3-[2-Fluoro-4-((2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenylamino]-propyl}-tetrahydro-pyran-4-carboxylic acid methyl ester (40 mg, 0.1 mmol, 1 eq) was dissolved in 2 mL of THF and cooled to 0° C., where a 2.5 M solution of n-BuLi in heptanes (0.11 mL, 0.17 mmol, 3 eq) was added drop-wise and the ice bath was removed. After 30 min the reaction mixture was quenched with water, transferred to a separatory funnel and extracted with diethyl ether (2×50 mL). The combined organics were dried over Na2SO4 and purified by column chromatography on silica gel (40 g column, 10% MeOH in CH2Cl2; 35 mL/min). This gave 38 mg (98%) of the title compound as an off-white gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383814B2
Source datasetuspto-grants-2013_02
ORD IDord-c982506dd75645f1b95169dd4f684d4e
Source noteuspto-grants-2013_02