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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959592Generated: October 31, 2026

Acetic Acid → [5-Chloro-4-(tetrahydro-pyran-2-yloxymethyl)-pyridin-3-ylmethyl]-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-amine

https://huagongshe.com/reaction/1959592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,3-Dioxolane-4-methanamine, 2,2-dimethyl-HCID 4122349—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-Chloro-4-(tetrahydro-pyran-2-yloxymethyl)-pyridine-3-carbaldehydeHCID 44190474—
SolventMethanolHCID 887—
Product[5-Chloro-4-(tetrahydro-pyran-2-yloxymethyl)-pyridin-3-ylmethyl]-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-amineHCID 67077614—

Reaction Steps

Acetic acid (133 μL) and NaBH3CN (14.8 mg, 0.235 mmol) were added to a stirred solution of 5-chloro-4-(tetrahydro-pyran-2-yloxymethyl)-pyridine-3-carbaldehyde (40 mg, 0.157 mmol) and 2,2-dimethyl-1,3-dioxolane-4-methanamine (203 μL, 1.57 mmol) in MeOH (1 mL). After stirring for 2 h at room temperature the solvent was removed in vacuo and the residue was partitioned between DCM (10 mL) and saturated NaHCO3 solution (10 mL). After extraction of the aqueous layer with DCM (2×10 mL) the combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The resulting title compound was used for the next reaction without purification. MS (m/z): 370.9 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410134B2
Source datasetuspto-grants-2013_04
ORD IDord-d243385d15174455806e5f9d7a8caae5
Source noteuspto-grants-2013_04