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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381059Generated: November 2, 2026

N,N-Dimethylcyclohexylamine → 2,5-Dimethyl-3-[(pyridin-3-yl)oxy]-1lambda~6~,2,4,6-thiatriazine-1,1(2H)-dione

https://huagongshe.com/reaction/1381059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylcyclohexylamineHCID 7415—
Reactant3-HydroxypyridineHCID 7971—
Reactant2H-1,2,4,6-Thiatriazine, 3-chloro-2,5-dimethyl-, 1,1-dioxideHCID 158865—
SolventDichloromethaneHCID 6344—
Product2,5-Dimethyl-3-[(pyridin-3-yl)oxy]-1lambda~6~,2,4,6-thiatriazine-1,1(2H)-dioneHCID 1330428668.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

17.1 parts of β-hydroxypyridine in 120 parts of methylene chloride and 19.1 parts of N,N-dimethylcyclohexylamine are introduced simultaneously, via 2 feeds, in the course of 15 minutes and at 15°-20° C., into a stirred solution of 29.3 parts of 2,5-dimethyl-3-chloro-2H-1,2,4,6-thiatriazine 1,1-dioxide in 150 parts of methylene chloride. The mixture is stirred for one hour at 25° C., after which the precipitate is filtered off under suction and the filtrate is washed with water and with dilute sodium carbonate solution, dried over magnesium sulfate, chromatographed over neutral aluminum oxide and then evaporated down under reduced pressure to give 26 parts (68.6% of theory) of 2,5-dimethyl-3-(pyrid-3-yloxy)-2H-1,2,4,6-thiatriazine 1,1-dioxide of melting point 137°-138° C. (compound No. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585472
Source datasetuspto-grants-1986_04
ORD IDord-9792fc34d7f3477c95387079944cfcc0
Source noteuspto-grants-1986_04