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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474283Generated: October 29, 2026

Hydrazine → 4-amino-1-(2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrophenoxy)butan-2-ol

https://huagongshe.com/reaction/474283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant2-(3-hydroxy-4-(2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrophenoxy)butyl)isoindoline-1,3-dioneHCID 66668498—
SolventEthanolHCID 702—
Product4-amino-1-(2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrophenoxy)butan-2-olHCID 6666574581.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 2-(3-hydroxy-4-(2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrophenoxy)butyl)isoindoline-1,3-dione (2.458 g, 5.62 mmol) in EtOH (28.1 mL) was added hydrazine (8.82 mL, 281 mmol). The mixture was heated at 50° C. for 1.5 h. The reaction mixture was cooled to rt and filtered. The filtrate was concentrated and taken up in CH2Cl2. Again, the solid was filtered off, and the filtrate was concentrated and purified by Prep-HPLC to obtain 4-amino-1-(2-(3-methyl-1H-1,2,4-triazol-1-yl)-5-nitrophenoxy)butan-2-ol (1.4 g, 81% yield). LC-MS (M+H)+=308.2 1H NMR (500 MHz, methanol-d4) δ 9.25 (s, 1H), 8.12 (d, J=2.1 Hz, 1H), 8.10-7.98 (m, 2H), 4.39-4.26 (m, 2H), 4.26-4.15 (m, 1H), 3.25-3.08 (m, 2H), 2.48 (s, 3H), 2.05-1.86 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637523B2
Source datasetuspto-grants-2014_01
ORD IDord-29edc8d8e915417f8bebfbf570135d6c
Source noteuspto-grants-2014_01