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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366821Generated: November 1, 2026

1,3-Propanediamine → HCID 57718193, compound

https://huagongshe.com/reaction/1366821

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediamineHCID 428—
ReactantSodium IodideHCID 5238—
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 2-amino-5-bromoisonicotinateHCID 25307230—
CatalystCopper iodideHCID 83717—
Solvent1-PentanolHCID 6276—
ProductHCID 57718193HCID 5771819358%

Reaction Steps

2-amino-5-bromo-isonicotinic acid methyl ester (1.79 g, 7.75 mmol) was added to a stirred mixture of copper iodide (145 mg, 0.76 mmol), sodium iodide (2.36 g, 15.73 mmol) and 1,3-diaminopropane (0.13 ml, 1.55 mmol) in n-pentanol (20 ml) and heated to reflux overnight. The reaction was cooled to room temperature, ethyl acetate (100 ml) added and washed with NaHCO3 solution (50 ml) and brine (50 ml) before being dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography using ethyl acetate 1/4 hexane as eluent to afford 2-amino-5-iodo-isonicotinic acid pentyl ester as a yellow solid (1.51 g, 58%). 1H NMR (CDCl3): 8.36 (1 H, s, py); 6.77 (1 H, s, py); 4.50 (2 H, br s, NH2); 4.24 (2 H, t, OCH2); 1.72 (2 H, m, OCH2CH2); 1.32 (4 H, m, OCH2CH2CH2CH2CH3); 0.81 (3 H, t, CH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893077B2
Source datasetuspto-grants-2011_02
ORD IDord-0b145ad523ed42d09a276ce2f8de7648
Source noteuspto-grants-2011_02