GB815203A - Substituted-4-metathiazanones - Google Patents

Substituted-4-metathiazanones

Info

Publication number
GB815203A
GB815203A GB2099357A GB2099357A GB815203A GB 815203 A GB815203 A GB 815203A GB 2099357 A GB2099357 A GB 2099357A GB 2099357 A GB2099357 A GB 2099357A GB 815203 A GB815203 A GB 815203A
Authority
GB
United Kingdom
Prior art keywords
chlorophenyl
dichlorophenyl
phenyl
methyl
metathiazanones
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB2099357A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
STWB Inc
Original Assignee
Sterling Drug Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sterling Drug Inc filed Critical Sterling Drug Inc
Publication of GB815203A publication Critical patent/GB815203A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D279/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
    • C07D279/041,3-Thiazines; Hydrogenated 1,3-thiazines
    • C07D279/061,3-Thiazines; Hydrogenated 1,3-thiazines not condensed with other rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

The invention comprises compounds of the general formula <FORM:0815203/IV (b)/1> wherein Z is S or SO2; Ar is an aromatic radical, including substituted or unsubstituted phenyl, naphthyl, biphenylyl, furyl, pyridyl and thienyl radicals; R is H or a lower hydrocarbyl radical having an aliphatic carbon atom linked to the ring-nitrogen atom (containing 1-8 carbon atoms); R1, R2 and R3 are each H or a lower alkyl radical (containing 1-3 carbon atoms) and the manufacture thereof by heating an aldehyde of the formula Ar-CAO, a betamercapto propionic acid of the general formula HS.CH(R1)C(R2)(R3)COOH and an aminating agent, i.e. a compound having a high ammonia partial pressure which usually loses ammonia on standing and which readily decomposes when heated to lose ammonia, or a hydrocarbylamine of the general formula R-NH2 and, if desired, oxidizing (for example, by potassium permanganate, hydrogen peroxide or chromium trioxide) the resulting compound where Z is S to the analogue where Z is SO2. Examples are given of the preparation of 2-(3,4-dichlorophenyl) - 3 - methyl - 4 - metathiazanone by reacting 3,4-dichlorobenzaldehyde, beta-mercaptopropionic acid and methylamine; of 2-(2,4-dichlorophenyl) -, 2 - (4 - isopropylphenyl) -, 2-(4 - chlorophenyl) -, 2 - (4 - methoxyphenyl)-, 2 - phenyl -, 2 - (2 - chlorophenyl) -, 2 - (3-chlorophenyl) -, 2 - (2 - thienyl) -, and 2 - (3-pyridyl) - 3 - methyl - 4 - metathiazanones, 4-(4 - chloro phenyl) - 3 - ethyl -, 2 - (4 - chlorophenyl) - 3 - n - propyl and 2 - phenyl - 3-benzyl - 4 - metathiazanones by a similar method using the appropriately substituted benzaldehyde and amine; of 2-phenyl-, 2-(4-methoxyphenyl) -, 2 - (4 - bromophenyl) -, 2-(3,4 - dichlorophenyl) -, 2 - (2,4 - dichlorophenyl)-, and 2-(4-chlorophenyl)-4-metathiazanones by reacting the corresponding aldehyde with ammonium carbonate, or carbamate, and betamercaptopropionic acid or its ammonium salt alone, whilst similarly may be prepared 2 - (3 - chlorophenyl) - 5 - methyl -, 2-(3,4 - dibromophenyl) - 6 - methyl -, 2 - (3,4 - dichlorophenyl) - 5 - ethyl - 6 - n - propyl -, 2 - (4-iodophenyl) -, 2 - (4 - fluorophenyl) -, 2 - (2,4,6-trichlorophenyl) - 5,6 - dimethyl -, 2 - (4 - isobutoxyphenyl) - 5,5,6 - trimethyl -, 2 - (3,4,5-trimethylphenyl) - 5,5,6 - trimethyl -, 2 - (4-ethylphenyl) - 5,5 - diethyl -, 2 - (3 - ethyl - 4-isopropoxyphenyl) - 5 - isopropoxy -, 2 - (3-ethoxy - 4 - chlorophenyl) -, 2 - (3 - n - hexylphenyl) - 5 - methyl - 2 - (1 - naphthyl) -, and 2 - (2 - biphenylyl) - 4 - metathiazanones. Further examples are also given of the preparation of 2 - (4 - chlorophenyl) - and 2 - (3,4 - dichlorophenyl) - 3 - methyl - 4 - metathiazanone-1-dioxides by oxidizing the corresponding 4-metathiazanones with potassium permanganate in aqueous acetic acid and, using a similar process and the corresponding 4 - metathiazanones, of 2-(2,4-dichlorophenyl)-, 2-phenyl-, 2 - (4 - methoxyphenyl) -, 2 - (4 - isopropylphenyl) -, 2 - (2 - chlorophenyl) -, 2 - (3 - chlorophenyl) -, 2 - (2 - thienyl) -, and 2 - (3 - pyridyl)-3 - methyl - 4 - metathiazanone - 1 - dioxides, 2-(4 - chlorophenyl) - 3 - n - propyl -, 2 - (4 - chlorophenyl) - 3 - ethyl -, 2 - phenyl - 3 - benzyl -, 2-(3,4 - dichlorophenyl) -, 2 - (4 - chlorophenyl)-, 2 - (4 - bromophenyl) -, and 2 - phenyl - 4-metathiazanone-1-dioxides.ALSO:Tablets, capsules, solutions and suspensions for oral or injectable administration may contain <FORM:0815203/VI/1> wherein Z is S or SO2; Ar is an aromatic radical, including substituted or unsubstituted phenyl, naphthyl, biphenylyl, furyl, pyridyl, and thienyl radicals; R is H, or a lower hydrocarbyl radical having an aliphatic carbon atom linked to a ring-nitrogen atom and containing 1-8 carbon atoms; R1-3 are each H, or a lower alkyl radical containing 1-3 carbon atoms, either alone or in combination with one or other medicinals such as asprin, phenacetin, salicylamide, para-acetylaminophenol, caffeine, and meperidine. Tablets may contain as adjuvants, calcium carbonate, starch, gelatin talc, magnesium stearate or acacia, and solutions and suspension may be made in water, alcohol/water oil or oil/water emulsions.
GB2099357A 1956-07-20 1957-07-03 Substituted-4-metathiazanones Expired GB815203A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US59901156A 1956-07-20 1956-07-20

Publications (1)

Publication Number Publication Date
GB815203A true GB815203A (en) 1959-06-17

Family

ID=24397835

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2099357A Expired GB815203A (en) 1956-07-20 1957-07-03 Substituted-4-metathiazanones

Country Status (3)

Country Link
CH (1) CH367826A (en)
DE (1) DE1111192B (en)
GB (1) GB815203A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3093639A (en) * 1961-07-27 1963-06-11 Sterling Drug Inc 2, 3-disubstituted-4-metathiazanones, -1-oxides and -1, 1-dioxides
US3155655A (en) * 1964-11-03 Dh chj
US3244703A (en) * 1961-10-19 1966-04-05 Shell Oil Co Thiazine, thiazoline, and thiazolinone compounds
CN104817518A (en) * 2014-09-23 2015-08-05 河南九势制药股份有限公司 Optimized chlormezanone synthesis method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2585064A (en) * 1952-02-12 Meta-thiazines

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3155655A (en) * 1964-11-03 Dh chj
US3093639A (en) * 1961-07-27 1963-06-11 Sterling Drug Inc 2, 3-disubstituted-4-metathiazanones, -1-oxides and -1, 1-dioxides
US3244703A (en) * 1961-10-19 1966-04-05 Shell Oil Co Thiazine, thiazoline, and thiazolinone compounds
CN104817518A (en) * 2014-09-23 2015-08-05 河南九势制药股份有限公司 Optimized chlormezanone synthesis method

Also Published As

Publication number Publication date
DE1111192B (en) 1961-07-20
CH367826A (en) 1963-03-15

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