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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323450Generated: October 30, 2026

1,2-Hydrazinedicarboxaldehyde → methyl 2-methoxy-5-(4H-triazol-1-yl)benzoate

https://huagongshe.com/reaction/323450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-HydrazinedicarboxaldehydeHCID 12342—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantMethyl 5-amino-o-anisateHCID 89843—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethane methanolHCID 21226129—
SolventDichloromethane ethylacetateHCID 21226138—
Productmethyl 2-methoxy-5-(4H-triazol-1-yl)benzoateHCID 22009369—

Reaction Conditions

Temperature160 °C

Reaction Steps

Alternately, according to the method of J. Med. Chem., 21, 1100 (1978), combine methyl 2-methoxy-5-aminobenzoate (1.8 g, 10 mmol), diformyl hydrazine (0.97 g, 11 mmol), and phosphorous pentoxide (1.84 g, 13 mmol). Heat to 160° C. After 1.5 hours, cool the reaction mixture and add a saturated aqueous solution of sodium bicarbonate. Extract three times with dichloromethane. Dry the combined organic layers over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 40% ethyl acetate/dichloromethane and then 5% methanol/dichloromethane to give methyl 2-methoxy-5-(4H-triazol-1-yl)benzoate: mp; 179-182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-51d4e5ada01148b294c4f63a0dbc22fa
Source noteuspto-grants-2001_04