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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374230Generated: October 27, 2026

Water → 6-Methyl-3-[1-(4-nitrophenoxy)tridecyl]-7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazine

https://huagongshe.com/reaction/374230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsopropanolHCID 3776—
Reactant2-(2-[4-nitrophenoxy] tetradecanoyl)-1-(5-methyl 6H-1, 3,4 thiadiazin-2-yl)hydrazineHCID 54096145—
SolventAcetic AcidHCID 176—
Product6-Methyl-3-[1-(4-nitrophenoxy)tridecyl]-7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazineHCID 1500271685.6%

Reaction Conditions

Temperature95 °C

Reaction Steps

A solution of 33.0 g of the above substituted acylhydrazine 1b in 132 ml of acetic acid is heated with stirring at 95° C. for 2 hours. At the end of the reaction, 65 ml of isopropyl alcohol is added to the reaction mixture. And then the whole mixture is added with stirring to 200 ml of 70° C. water. After cooling to 20° C. and stirring at that temperature for an hour, the product is collected, washed with water, dried, and recrystallized from isopropyl alcohol to give 27.2 g (47% overall from 3b or 86% from 1b) of 6-methyl3-(1-[4-nitrophenoxy]tridecyl)-7H-1, 2,4 triazolo(3,4-b)-1,3,4 -thiadiazine (4) with 95 area % by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166378
Source datasetuspto-grants-1992_11
ORD IDord-b7b2daac92b8479097a044285690b196
Source noteuspto-grants-1992_11