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HRID 1948121Erstellt: 26. Oktober 2026

Hydrochloric Acid → Diethyl[(6-amino-5-methoxypyridin-3-yl)methyl]phosphonate

https://huagongshe.com/reaction/1948121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhosphonic acid, P-(chloromethyl)-, diethyl esterHCID 76633—
Edukt3-Methoxy-2-nitropyridineHCID 556063—
Eduktsodium 2-methylpropan-2-olateHCID 178418730—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktDiethyl[(6-amino-5-methoxypyridin-3-yl)methyl]phosphonateHCID 8665406519,2%

Reaktionsschritte

A solution of 2-nitro-3-methoxypyridine (300 mg, 1.95 mmol) and diethyl chloromethylphosphonate (363 mg, 1.95 mmol) in DMSO (4 mL) was added dropwise to vigorously stirred solution of t-BuONa (0.561 g, 5.84 mmol) in DMSO (4 mL) at room temperature. The reaction mixture turned to deep orange immediately. Stirring was continued for 30 min, then the mixture was poured into 1 M HCl (aq) (10 mL). The product was extracted into ether (3×30 mL), dried over MgSO4, concentrated, and purified by silica gel chromatography (3% MeOH in DCM) to afford 102.6 mg of diethyl[(6-amino-5-methoxypyridin-3-yl)methyl]phosphonate (yield: 17%). 1H NMR (CD3OD, 400 MHz): δ=1.30 (t, J=6.8 Hz, 6H), 3.45 (d, J=22.4 Hz, 2H), 4.00 (s, 3H), 4.09-4.17 (m, 4H), 7.79 (t, J=2.4 Hz, 1H), 7.97 (t, J=2.4 Hz, 1H). MS (ES+): m/z 305.07 [MH+]. HPLC: tR=1.17 min (UPLC TOF, polar—3 min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08399433B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-38df4a388e804322a0c06b393ec59d54
Quellennotizuspto-grants-2013_03