Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916474Generated: October 30, 2026

Cyclopentanecarbaldehyde → 1-(5-bromopyridin-3-yl)-N-(cyclopentylmethyl)methanamine

https://huagongshe.com/reaction/1916474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanecarbaldehydeHCID 70106—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(Aminomethyl)-5-bromopyridineHCID 22992264—
SolventMethanolHCID 887—
Product1-(5-bromopyridin-3-yl)-N-(cyclopentylmethyl)methanamineHCID 8669832779.3%

Reaction Steps

A solution of (5-bromopyridin-3-yl)methanamine (LVIII) (1.30 g, 5.8 mmol, 1.0 eq), cyclopentanecarbaldehyde (0.57 g, 5.8 mmol, 1.0 eq) and TEA (0.60 g, 5.8 mmol, 1.0 eq) in MeOH (15 mL) was stirred at room temperature for 2 h. Then NaBH3CN (1.98 g, 34.6 mmol, 6.0 eq) was added and the mixture was stirred at the same temperature for another 3 h. The solvent was removed under reduced pressure and the residue was diluted in water (20 mL) and extracted with DCM (10 mL×3), combined organic layers were dried over MgSO4 and concentrated in vacuo to give 1-(5-bromopyridin-3-yl)-N-(cyclopentylmethyl)methanamine (LIX) (1.23 g, 4.57 mmol, 79.3% yield) as a brown oil. ESIMS found for C12H17BrN2 m/z 269 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618128B1
Source datasetuspto-grants-2013_12
ORD IDord-b7f16c0f8cbf47e4aa42538b47c60f32
Source noteuspto-grants-2013_12