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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472169Generated: November 2, 2026

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

https://huagongshe.com/reaction/1472169

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 numberUS09012472B2
Source datasetuspto-grants-2015_04
ORD IDord-c936a2026950415ab2d4a85cd0a3015a
Source noteuspto-grants-2015_04