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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745887Generated: November 1, 2026

N,O-Dimethylhydroxylamine → HCID 13371782, compound

https://huagongshe.com/reaction/745887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,O-DimethylhydroxylamineHCID 14232—
Reactant6,8-Dimethyl-1H-1lambda~6~-pyrimido[1,2-b][1,2,4,6]thiatriazine-1,1,3(2H)-trioneHCID 13371774—
SolventDichloromethaneHCID 6344—
ProductHCID 13371782HCID 1337178267.8%

Reaction Steps

5.7 g (0.025 mol) of 2,3-dihydro-6,8-dimethyl-3-oxopyrimidino-[1,2-b][1,2,4,6]-thiatriazine 1,1-dioxide (cf. Example 1) are suspended in 100 ml of methylene dichloride, and 3.05 g (0.05 mol) of O,N-dimethylhydroxylamine--dissolved in 50 ml of methylene dichloride--are added at -40° C. in the course of one hour. The mixture is stirred for a further 18 hours at room temperature and evaporated to dryness, and the residue is taken up in water and acidified to pH 4--5 with 0.5 N HCl. After extraction with methylene dichloride, the mixture is worked up as under Example 17. 4.9 g (67.8% of theory) of 1-[(N-methoxy-N-methylamino)-sulfonyl]-3-(4,6-dimethyl-2-pyrimidinyl)-urea of melting point 152° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04601747
Source datasetuspto-grants-1986_07
ORD IDord-dcd47163bf4449559e8b6806395e4f7f
Source noteuspto-grants-1986_07