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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17981Generated: October 26, 2026

Ethanol → 2-(5-Oxo-3-thioxo-2,3,4,5-tetrahydro-[1,2,4]triazin-6-ylmethyl)indan-1,3-dione

https://huagongshe.com/reaction/17981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiisopropylethylamineHCID 81531—
ReactantThiosemicarbazideHCID 2723789—
ReactantEthyl 3-(1,3-dioxoisoindolin-2-yl)-2-oxopropanoateHCID 57680977—
Product2-(5-Oxo-3-thioxo-2,3,4,5-tetrahydro-[1,2,4]triazin-6-ylmethyl)indan-1,3-dioneHCID 86602721—

Reaction Conditions

Temperature80 °C

Reaction Steps

A slurry of 3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-oxo-propionic acid ethyl ester (20 g, 76.6 mmol) in anhydrous EtOH (300 mL) was charged with thiosemicarbazide (6.98 g, 76.6 mmol) in one portion and heated to 80° C. for 2 h. The reaction mixture was charged with N,N′-diisopropylethylamine (DIEA) (26.7 mL, 76.56 mmol) and heated to 40° C. for 6 h then stirred at rt for an additional 10 h. The reaction mixture was concentrated in vacuo and solid was triturated with hot EtOH/EtOAc filtered and washed with EtOAc. The solid was dried overnight in a vacuum oven (40° C.) resulting in the title compound as an off-white solid; 1H NMR (DMSO-d6, 400 MHz) δ 4.68 (s, 2H), 7.85-7.95 (m, 4H); MS (ES+): m/z 289.2 (100) [MH+], HPLC: tR=2.50 min (MicromassZQ, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741324B2
Source datasetuspto-grants-2010_06
ORD IDord-9400516d6b1d4aa29d5b4216bcae10d6
Source noteuspto-grants-2010_06