GB522531A - - Google Patents

Info

Publication number
GB522531A
GB522531A GB522531DA GB522531A GB 522531 A GB522531 A GB 522531A GB 522531D A GB522531D A GB 522531DA GB 522531 A GB522531 A GB 522531A
Authority
GB
United Kingdom
Prior art keywords
methyl
aminopyrimidine
ethoxymethyl
dec
prepared
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
Other languages
English (en)
Publication date
Publication of GB522531A publication Critical patent/GB522531A/en
Expired legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
GB522531D Expired GB522531A (enExample)

Publications (1)

Publication Number Publication Date
GB522531A true GB522531A (enExample) 1900-01-01

Family

ID=1748019

Family Applications (1)

Application Number Title Priority Date Filing Date
GB522531D Expired GB522531A (enExample)

Country Status (1)

Country Link
GB (1) GB522531A (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1150987B (de) * 1960-07-28 1963-07-04 Knoll Ag Verfahren zur Herstellung von 2-Methyl-4-amino-5-chlormethyl-pyrimidin-hydrochlorid
DE1294384B (de) * 1959-11-20 1969-05-08 Merck & Co Inc Verfahren zur Herstellung von 1-(2-Alkyl-4-amino-5-pyrimidyl-methyl)-pyridiniumhalogeniden

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1294384B (de) * 1959-11-20 1969-05-08 Merck & Co Inc Verfahren zur Herstellung von 1-(2-Alkyl-4-amino-5-pyrimidyl-methyl)-pyridiniumhalogeniden
DE1150987B (de) * 1960-07-28 1963-07-04 Knoll Ag Verfahren zur Herstellung von 2-Methyl-4-amino-5-chlormethyl-pyrimidin-hydrochlorid

Similar Documents

Publication Publication Date Title
FI114010B (fi) Menetelmä kasvainsairauksien parantamiseen tarkoitettujen farmaseuttisten tuotteiden valmistamiseksi
Tronche et al. Polar substituent and solvent effects on the kinetics of radical reactions with thiols
Wynne et al. Physiological studies on spore germination, with special reference to Clostridium botulinum: III. Carbon dioxide and germination, with a note on carbon dioxide and aerobic spores
ES2190794T3 (es) Procedimiento para la preparacion de disoluciones acuosas de dioxido de cloro.
CN102124120B (zh) 透明质酸的制备方法
Beach et al. Investigations of structures of substituted lumazines by deuterium exchange and nuclear magnetic resonance spectroscopy
GB522531A (enExample)
Wiame et al. Oxidative assimilation by Pseudomonas saccharophila with C14-labeled substrates
Subbarow et al. Pantothenic acid as a factor in rat nutrition
CN108017561A (zh) 一种精制卡谷氨酸的方法
Riley et al. Metabolism of ciliary body in relation to formation of aqueous humour
Ogata et al. Microbial formation of cinnamic acid from phenylalanine
Houlahan et al. Evidence for an Interrelation in the Metabolism of Lysine, Arginine and Pyramidines in Neurospora
US6518247B1 (en) Method for producing an antitumoral agent and antitumoral agent thus obtained
ATE63318T1 (de) Immunosuppressive verbindungen, deren mikrobiologische verfahren zur herstellung und deren verwendung als arzneimittel.
JPH02219582A (ja) 発酵法によるl―スレオニンの製造法
CN117731607A (zh) 一种硝普钠注射液及其制备方法
CN110921924A (zh) 一种叶酸废水的环保处理方法
McCOY et al. Some factors affecting the nutritional requirements of Streptococcus faecalis
US3058888A (en) Process for producing alpha-isoleucine
GB1375189A (en) Process and apparatus for producing single-cell protein materials
KUWADA et al. On the biosynthesis of riboflavin in the culture of Eremothecium ashbyii
GB1384194A (en) Process for the production of trisodium or tripotassium citrate
Trudinger The synthesis of indole from anthranilic acid by Escherichia coli
CN110606495B (zh) 一种提升单氰胺产品品质的方法