Nitrogen → 2-((5-(methoxymethyl)furan-2-yl)methyl)-2H-1,2,3-triazol-4-amine

Temperature

90 °C

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a mixture of 2-((5-(methoxymethyl)furan-2-yl)methyl)-4-nitro-2H-1,2,3-triazole (97 mg, 0.35 mmol), iron powder (59 mg, 1.04 mmol) and NH4Cl (94 mg, 1.74 mmol) in a mixture of EtOH (1.6 mL) and water (0.8 mL) was stirred at 90° C. for 2 h. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (20 mL) was added followed by 1N NaOH (10 mL). The layers were separated and the aq. layer was extracted with CH2Cl2 (10 mL). The combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (95:5 CH2Cl2-MeOH) gave the title compound as a yellow oil: TLC: rf (95:5 CH2Cl2-MeOH)=0.39. LC-MS-conditions 07: tR=0.51 min, [M+H]+=209.34.

1. filtrationThe reaction mixture was filtered while hot and
2. concentrationconcentrated under reduced pressure
3. additionCH2Cl2 (20 mL) was added
4. customThe layers were separated
5. extractionthe aq. layer was extracted with CH2Cl2 (10 mL)
6. dry with materialextracts were dried over Na2SO4
7. filtrationfiltered
8. customthe solvents were removed under reduced pressure
9. customPurification of the residue by FC (95:5 CH2Cl2-MeOH)

ORD record

ord-f1583d0dbdcc4a6e816c474198fa3169

Source dataset

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08846733B2