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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water ethanol | HCID 19096565 | — |
| Reactant | (S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzaldehyde | HCID 86696106 | — |
| Product | 1-[(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperidine-4-carboxylic acid | HCID 68359044 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946203B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-3ac42f74dabf4ea391d037e86f9d3454 |
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| Source note | uspto-grants-2015_02 |
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