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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841973Generated: October 31, 2026

Water ethanol → 1-[(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1841973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWater ethanolHCID 19096565—
Reactant(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzaldehydeHCID 86696106—
Product1-[(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperidine-4-carboxylic acidHCID 68359044—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1-[(8)-4-(2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperidine-4-carboxylic acid ethyl ester (prepared from Intermediate C and piperidine-4-carboxylic acid ethyl ester according to General Method F) (3.00 g, 7.90 mmol) in 4:1 EtOH/water (80 mL) is added LiOH monohydrate (0.994 g, 23.7 mmol) and the reaction stirred overnight at about 25° C. The reaction is concentrated, diluted with water and washed with Et2O (2×). The aqueous layer is lypholized to dryness then purified by silica gel chromatography eluting with 20% (2M NH3 in MeOH)/DCM. The pooled fractions are concentrated and dried to provide the title compound (K) as a foamed solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946203B2
Source datasetuspto-grants-2015_02
ORD IDord-3ac42f74dabf4ea391d037e86f9d3454
Source noteuspto-grants-2015_02