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1.2.6- Thiadiazin

Under acidic conditions, a thiosemicarbazone intermediate (145) has been isolated, this can be cyclized in alcohol either into the corresponding 2-hydrazinothiazole (142) in the presence of benzaldehyde or into 1,3,4-thiadiazine (146) in the absence of benzaldehyde (Scheme 71) (375, 397, 408). [Pg.249]

DiaminO 4,4-dimethyl-l,3,5-thiadiazine hydrobromide was isolated as by-product (418). Benzene sulfonates of cyanohydrin prepared from sodium cyanide and an halobenzoaldehyde, when treated with thiourea or its derivatives, afford 2,4-diamino-5-(p-halogenophenyl)-thiazole benzene sulfonates (447). Similarly, cyanoamido thiocarbamates obtained from cyanamide and isothiocyanates yield substituted 2,4-diaminothiazoles (598). [Pg.297]

Another example is a claim of possible industrial appHcation for preparing l-cyclohexyl-3,5-dimethylpyrazole [79580-49-7] (75) and similar compounds from 1,2,6-thiadiazine-l,1-dioxide (74) by extmsion of SO2 (eq. 20) (48). This process has the added advantage of not requiring hydrazine derivatives as reactants. [Pg.316]

Chloromethylbenzo-l,2,4-thiadiazine 1,1-dioxide forms quaternary salts, e.g. 8 (n = 1), with pyridine, 2- and 3-picolines, and iso-quinoljne, but the 3-(2 -chloroethyl) compound gives a lower yield of the salt, e.g. 8 (% = 2), because some of the halogen derivative is converted into the 3-vinyl compound. ... [Pg.6]


See other pages where 1.2.6- Thiadiazin is mentioned: [Pg.102]    [Pg.974]    [Pg.134]    [Pg.123]    [Pg.274]    [Pg.287]    [Pg.37]    [Pg.61]    [Pg.61]    [Pg.61]    [Pg.61]    [Pg.61]    [Pg.61]    [Pg.61]    [Pg.663]    [Pg.663]    [Pg.663]    [Pg.719]    [Pg.719]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.859]    [Pg.866]    [Pg.914]    [Pg.914]    [Pg.339]    [Pg.387]    [Pg.8]    [Pg.369]   
See also in sourсe #XX -- [ Pg.498 ]




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1 //-Pyrazino thiadiazine

1,2,3-Thiadiazine 1-oxides

1,2,6-Thiadiazine 1,1-dioxides aromaticity

1,2,6-Thiadiazine 1,1-dioxides reduction

1,2,6-Thiadiazine 1,1-dioxides structure

1,2,6-Thiadiazine 1,1-dioxides synthesis

1,2,6-Thiadiazine-1,1 -diones

1,2,6-Thiadiazine-1,1 -diones synthesis

1,2,6-Thiadiazines, tautomerism

1,3,4-Thiadiazines, review

1,3,4-Thiadiazines, tetrahydro-, conformation

1,3,5-thiadiazines

1.2.3- Thiadiazines, monocyclic

1.2.3- Triazino thiadiazines

1.2.4- Thiadiazine 5-imines

1.2.4- Thiadiazines applications

1.2.4- Thiadiazines literature

1.2.4- Thiadiazines spectra

1.2.4- Triazolo thiadiazine

1.2.4- Triazolo thiadiazines

1.2.5- Thiadiazines reactivity

1.2.5- Thiadiazines structure

1.2.6- Thiadiazin-3-one 1,1-dioxides

1.2.6- Thiadiazine-3,5-dione 1,1-dioxides

1.2.6- Thiadiazines, 1-oxides, 1,1-dioxides

1.3.4- Thiadiazin-5 -ones

1.3.4- Thiadiazines, fused

1.3.4- Thiadiazines, fused synthesis

1.3.5- Thiadiazines from thioureas

1/7-2,1,4-Benzo thiadiazines

2- Substituted-5-phenyl-6//-1,3,4-thiadiazine

2//-l,3,5-Thiadiazines

2H-l,3,5-Thiadiazin-2-ones

3.5- Dimethyl-tetrahydro-1,3,5-thiadiazine-2-thione

4//-l,2,4-Thiadiazine

4H-1,3,5-Thiadiazin-4-ones

4H-l,3,4-Thiadiazin-5-ones

4H-l,3,5-Thiadiazine-4-thiones

Amino-substituted 1,2,6-thiadiazine

Amino-substituted 1,2,6-thiadiazine 1,1-dioxides, tautomerisation

Amino-substituted 2,1,3-thiadiazine 1,1-dioxides

Aminopyrido -l,2,6-thiadiazine

Aminopyrido -l,2,6-thiadiazine 2,2-dioxides, protonation

Benzo-l,2,4-thiadiazine 1,1-dioxides

Busby, R. E., Thiadiazines with Adjacent

Busby, R. E., Thiadiazines with Adjacent Sulfur

Busby, R. E., Thiadiazines with Adjacent Sulfur and Nitrogen Ring Atoms

Herbicidal thiadiazine dioxides

Isothiocyanates 1.3.5- thiadiazine-2-thiones

L,3,5-Thiadiazine-2-thiones

Naphtho thiadiazines

Pyrazino thiadiazine 2,2-dioxides

Pyrazino thiadiazines

Pyrazole from thiadiazine 1-oxides

Pyrazoles 1,3,4-thiadiazines

Pyrazolo 1,2,4-thiadiazines

Pyrido thiadiazine 2,2-dioxides

Sulfur extrusion from 1,2,6-thiadiazines

Tetrahydro-1,2,4-thiadiazine 1,1-dioxide

Tetrahydro-1,3,4-thiadiazines

Tetrahydro-3,5,dimethyl-2H-l,3,5-thiadiazine-2-thione

Tetrahydro-3,5-dimethyl-2H-l,3,5-thiadiazine

Tetrahydro-l,3,5-thiadiazines

Thiadiazine

Thiadiazine derivatives

Thiadiazine dioxides

Thiadiazine dioxides tautomerism

Thiadiazine dioxides, formation

Thiadiazines with adjacent sulfur and

Thiadiazines with adjacent sulfur and nitrogen

Thiadiazines with adjacent sulfur and nitrogen ring atoms

Thiadiazines, synthesis

Thiazolines 1.3.4- thiadiazines

Thiazolines 1.3.4- thiadiazines, 2-amino

Thiazolo thiadiazin-6 -ones

Thiazolo thiadiazine

Thiazolo thiadiazines

Thieno -1,2,4-thiadiazines

Thieno thiadiazine

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