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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441850Generated: October 30, 2026

HCID 21875453, compound → 5-Amino-3-methoxypyridine-2-carbonitrile

https://huagongshe.com/reaction/1441850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21875453HCID 21875453—
CatalystIronHCID 23925—
SolventEthyl acetate acetateHCID 22609514—
Product5-Amino-3-methoxypyridine-2-carbonitrileHCID 2187533697%

Reaction Conditions

Temperature65 °C

Reaction Steps

2-Cyano-3-methoxy-5-nitropyridine (1.0 g, 5.6 mmol) was dissolved in 1:1 EtOAc/AcOH (10 mL) and heated to 65° C. Iron powder (1.61 g, 28 mmol, 325 mesh) was added and the mixture stirred for two h. The mixture was filtered though Celite and the filtrate concentrated in vacuo. The residue was partitioned between EtOAc and saturated aqueous sodium bicarbonate. The organic layer was separated, washed with brine, dried (MgSO4), filtered and concentrated. The residue was purified by SiO2 Prep-TLC using CH2Cl2 as the eluent to give the compound 762D (0.805 g, 97%) as an off-white solid. HPLC: 100% at 1.31 min(YMC S5 ODS column) eluting with 10-90% aqueous methanol containing 0.2% phosphoric acid over a 4 min gradient monitoring at 220 nm. MS (ES): m/z 149.90 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655689B2
Source datasetuspto-grants-2010_02
ORD IDord-d0914536f518468eba6bc57b09012b82
Source noteuspto-grants-2010_02