GB927699A - - Google Patents
Info
- Publication number
- GB927699A GB927699A GB927699DA GB927699A GB 927699 A GB927699 A GB 927699A GB 927699D A GB927699D A GB 927699DA GB 927699 A GB927699 A GB 927699A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphapyrimidines
- group
- alkoxy
- alkoxy group
- nov
- 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.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/69—Benzenesulfonamido-pyrimidines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
927,699. Sulphapyrimidines. F. HOFFMANN-LA ROCHE & CO. A.G. Nov. 18, 1960 [Nov. 18, 1959; Jan. 14, 1960], No. 39695/60. Class 2(3). The invention comprises sulphapyrimidines of the general formula (wherein R<SP>1</SP> is a hydrogen atom or an acyl group and R<SP>2</SP> is an alkylthio group containing up to six carbon atoms or an alkoxy group), and a process for the preparation of sulphapyrimidines of the general formula (wherein R<SP>3</SP> is a halogen atom or, when R<SP>2</SP> is an alkoxy group, an alkoxy group) by reacting a 2-R<SP>2</SP>-4,6-dihalopyrimidine with an alkali metal salt of sulphanilamide or an N-acyl derivative thereof and, if desired, hydrolysing the N<SP>1</SP>-acyl group (if present) in the product and, if desired, replacing the remaining halogeno substituent and any alkylthio group by alkoxy. 2-Methoxy-4.6-dihydroxypyrimicidine is prepared by treating O-methylurea chloride with sodium methoxide followed by dimethyl malonate, and is converted to 2-methoxy-4.6- dichloropyrimidine by treatment with phosphorus oxychloride in the presence of dimethylaniline.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB927699T |
Publications (1)
Publication Number | Publication Date |
---|---|
GB927699A true GB927699A (en) |
Family
ID=10728012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB927699D Active GB927699A (en) |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB927699A (en) |
MY (1) | MY6400035A (en) |
-
0
- GB GB927699D patent/GB927699A/en active Active
-
1964
- 1964-12-31 MY MY6400035A patent/MY6400035A/en unknown
Also Published As
Publication number | Publication date |
---|---|
MY6400035A (en) | 1964-12-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Swedes et al. | Relation of growth and protein synthesis to the adenylate energy charge in an adenine-requiring mutant of Escherichia coli. | |
ZA967365B (en) | Process for the preparation of quinazoline derivatives. | |
PL331599A1 (en) | Substituted derivatives of pyrimidine and their pharmaceutical application | |
Kaboudin | A simple and new method for the synthesis of thiophosphates | |
GB927699A (en) | ||
US3814761A (en) | (2-pyrimidinylthio)alkanoic acids,esters,amides and hydrazides | |
GB2015995A (en) | Herbicidal 4-(2-pyridyloxy)- phenoxy valeric acid derivatives | |
Davidson | Specificity of pyruvate kinase | |
IL70767A0 (en) | Analogs of mevalonolactone and derivatives thereof,their production and pharmaceutical compositions containing them | |
ES8604943A1 (en) | Desoxyuridine derivatives, processes for their preparation and their use as pharmaceuticals | |
ES472182A1 (en) | Amino-2 (or -4) alkylthio-5 pyrimidines, processes for their preparation, their use as herbicides and composition containing them. | |
Gassman et al. | A comparison of the heterolytic vs. homolytic cleavage of the nitrogen-chlorine bond | |
Heaton et al. | The structural specificity of the nucleotide-binding site and the reversible nature of the inhibition of proton conductance induced by bound nucleotides in brown-adipose-tissue mitochondria | |
GB1157666A (en) | A Method for the Production of a 5'-Ribonucleotide | |
TW325463B (en) | 4-Aminobenzoylguanidine-derivatives | |
ES8307185A1 (en) | Hydrogen peroxide adduct, process for its manufacture and its use. | |
AU4708289A (en) | Process for the preparation of pyrimidine derivatives | |
US3940394A (en) | 2-pyrimidinylthio)alkanoic acids, esters, amides and hydrazides | |
US5994540A (en) | Di-and trisubstituted pyridines and their preparation | |
ES8403469A1 (en) | Novel aniline derivatives, process for preparing the same and cardiotonic compositions containing the same. | |
Weidner et al. | Mixed thiolsulfonates and sulfonamides from polyfunctional mercaptans using trifluoromethyl thiosulfonates | |
GB684759A (en) | Improvements in and relating to the synthesis of derivatives of pyrimidine | |
IL74269A0 (en) | 2-alkoxyaminosulfonylbenzene-sulfonylureas,their production and their use as herbicides | |
ES8606302A1 (en) | Heterocyclic compounds, their preparation, compositions containing them and method of controlling unwanted plant growth. | |
GB774094A (en) | Improvements in or relating to pyrimidine compounds |