Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056624Generated: November 1, 2026

Methylamine → Tert-butyl 8-(methylamino)-2-azaspiro[4.5]decane-2-carboxylate

https://huagongshe.com/reaction/1056624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-Butyl 8-oxo-2-azaspiro[4.5]decane-2-carboxylateHCID 71711106—
ProductTert-butyl 8-(methylamino)-2-azaspiro[4.5]decane-2-carboxylateHCID 11839001475.7%

Reaction Steps

To a solution of methylamine (33% [w/w] in EtOH, 7.42 g, 79.0 mmol) was added tert-butyl 8-oxo-2-azaspiro[4.5]decane-2-carboxylate (4 g, 15.80 mmol), the reaction mixture was stirred at rt overnight. To the mixture was added NaBH3CN (2.98 g, 47.4 mmol), and the reaction mixture was stirred at rt for another 2 h and concentrated in vacuo. The residue was diluted with H2O (50 mL) and the resulting mixture was extracted with DCM (80 mL×3). The combined organic phases were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (DCM/MeOH (v/v)=10/1) to give the product as yellow oil (3.2 g, 75.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399637B2
Source datasetuspto-grants-2016_07
ORD IDord-fa19d250d0c1411f900afe2f44285643
Source noteuspto-grants-2016_07