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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921913Generated: October 29, 2026

Sodium triacetoxyborohydride → 4-([Methyl-(2-pyridin-4-ylpyrimidin-4-ylmethyl)amino]methyl}piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1921913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-((methylamino)methyl)piperidine-1-carboxylateHCID 21934652—
Reactant2-Pyridin-4-YL-pyrimidine-4-carbaldehydeHCID 53441768—
SolventDichloromethaneHCID 6344—
Product4-([Methyl-(2-pyridin-4-ylpyrimidin-4-ylmethyl)amino]methyl}piperidine-1-carboxylic acid tert-butyl esterHCID 11560339—

Reaction Steps

To a solution of 4-methylaminomethylpiperidine-1-carboxylic acid tert-butyl ester (37 mg, 0.16 mmol) in anhydrous CH2Cl2 (3 mL) was added 2-pyridin-4-yl-pyrimidine-4-carbaldehyde (Preparation 2, 30 mg, 0.16 mmol) followed by NaBH(OAc)3 (38 mg, 0.18 mmol). The mixture was stirred vigorously at rt for 24 h, before being partitioned between CH2Cl2 (30 mL) and H2O (20 mL). The aqueous phase was extracted with CH2Cl2 (20 mL), then the combined organics were washed with brine (20 mL), dried (MgSO4), filtered and concentrated in vacuo. Flash column chromatography (EtOAc) gave the title compound. RT=2.36 min; m/z (ES+)=398 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173807B2
Source datasetuspto-grants-2012_05
ORD IDord-4428db75a4794b72a76bd77038264b5e
Source noteuspto-grants-2012_05