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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695890Generated: November 1, 2026

2,3-Diaminopyridine → tert-Butyl 4-[(2-aminopyridin-3-yl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1695890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DiaminopyridineHCID 9956—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Solvent1,2-DichloroethaneHCID 11—
Producttert-Butyl 4-[(2-aminopyridin-3-yl)amino]piperidine-1-carboxylateHCID 2229321761.7%

Reaction Steps

To a solution of 2,3-diaminopyridine (3.0 g, 27.5 mmol) in DCE (45 ml) was added tert-butyl 4-oxopiperidine-1-carboxylate (5.75 g, 28.8 mmol) and the reaction mixture stirred for min at RT before the portion-wise addition of NaBH(Oac)3 (8.7 g, 41.7 mmol) and continued stirring at RT until the reaction judged complete by LCMS. The reaction was quenched with 5% NaOH, the layers separated and the organic layer was dried over Na2SO4. Evaporation gave the desired product as a brown solid (4.96 g). LC/MS (10% to 99%): M/Z (M+H)+ (obs)=293; tR=2.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163737B2
Source datasetuspto-grants-2012_04
ORD IDord-13691eb28d9e461da3de2f011c7fb27b
Source noteuspto-grants-2012_04