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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719749Generated: October 29, 2026

Sulfur → 5-(1-Methylpyrrolidin-2-yl)pyridine-3-carbaldehyde

https://huagongshe.com/reaction/719749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfurHCID 5362487—
ReactantHCID 58594484HCID 58594484—
SolventTolueneHCID 1140—
Product5-(1-Methylpyrrolidin-2-yl)pyridine-3-carbaldehydeHCID 2190188083.6%

Reaction Steps

A solution of (S)-5-(1-methylpyrrolidin-2-yl)-1,4-dihydropyridine-3-carbaldehyde IV (0.011 g, 0.044 mmol) and elemental sulfur (0.0015 g, 0.044 mmol) in 2 mL of toluene was refluxed for 1 day. After filtration through a pad of Celite, and evaporation of the solvent under reduced pressure, the crude material was purified by RPLC (silica gel, 5% EtOAc/hexanes then EtOAc) to afford 0.007 g (83%) of 5-(1-methylpyrrolidin-2-yl)pyridine-3-carbaldehyde V as a clear oil. IR (thin film, neat, NaCl): 2950, 1586, 1370, 1120 cm−1. 1H NMR (CDCl3, 300 MHz) δ 10.13–10.12 (m, 1 H), 8.97–8.96 (m, 1 H), 8.79 (s, 1 H), 8.18 (s, 1 H), 3.30–3.20 (m, 2 H), 2.38–1.67 (m, 4 H); 13C NMR (CDCl3, 100 MHz) δ 191.26, 154.81, 150.91, 135.13, 131.69, 68.53, 57.19, 40.64, 40.64, 35.66, 23.02. HRMS Calcd for C11H14N2O: 191.1184 [M+H]+. Found: 191.1182 [M+H]+. [α]23D−92 (c=0.2, CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132545B2
Source datasetuspto-grants-2006_11
ORD IDord-9172ac50b1064f0b882c1915c7ebb6ca
Source noteuspto-grants-2006_11