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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841979Generated: October 31, 2026

Hydrochloric Acid → (S)-3-(4-piperazin-1-ylmethyl-phenyl)-2,3-dihydro-[1,4]dioxino[2,3-b]pyridine

https://huagongshe.com/reaction/1841979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant4-[(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 86695362—
Solvent1,4-DioxaneHCID 31275—
Product(S)-3-(4-piperazin-1-ylmethyl-phenyl)-2,3-dihydro-[1,4]dioxino[2,3-b]pyridineHCID 86695358—

Reaction Steps

To a solution of 4-[(S)-4-(2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester (prepared from Intermediate C and piperazine-1-carboxylic acid tert-butyl ester according to General Method N) (7.32 g, 17.8 mmol) in 1,4-dioxane (200 mL) is added 4M HCl in 1,4-dioxane (22.2 mL, 88.9 mmol). The resulting slurry is stirred overnight. The reaction is poured into water (600 mL) and basified with 2M aqueous Na2CO3. The product is extracted with DCM, and the combined extracts washed with brine and dried over Na2SO4 to afford the title compound (S) as an oil that partially crystallizes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946203B2
Source datasetuspto-grants-2015_02
ORD IDord-4a4943d2ae7f474abe816fdcd40812af
Source noteuspto-grants-2015_02