GB1013164A - Processes for the production of 5-ribonucleotides and 2,3-o-alkylidene ribonucleosides - Google Patents

Processes for the production of 5-ribonucleotides and 2,3-o-alkylidene ribonucleosides

Info

Publication number
GB1013164A
GB1013164A GB1512263A GB1512263A GB1013164A GB 1013164 A GB1013164 A GB 1013164A GB 1512263 A GB1512263 A GB 1512263A GB 1512263 A GB1512263 A GB 1512263A GB 1013164 A GB1013164 A GB 1013164A
Authority
GB
United Kingdom
Prior art keywords
phosphoryl chloride
hydrolysed
ketone
ribonucleosides
alkylidene
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
GB1512263A
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co 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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Publication of GB1013164A publication Critical patent/GB1013164A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/06Pyrimidine radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00Processes for the preparation of sugar derivatives
    • C07H1/02Phosphorylation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Saccharide Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Ribonucleosides are reacted with phosphoryl chloride or "hydrolysed phosphoryl chloride" in the presence of a ketone. If the mole ratio of ketone to phosphoryl chloride is less than 5, a 21,31 - alkylideneribonucleoside - 51 - phosphorochloridate is formed and this is hydrolysed with water to form the 21,31-O-alkylidene-51-ribonucleotide which is in turn hydrolysed to the 51-ribonucleotide in aqueous acid medium. If the mole ratio of ketone to phosphoryl chloride is greater than 5, a 21,31-O-alkylideneribonucleoside is obtained; if the excess ketone is then removed and further phosphoryl chloride added and optionally a proton acceptor, the product may be phosphorylated and then hydrolysed as in the first embodiment. The "hydrolysed phosphoryl chloride" consists predominantly of orthophosphorodichloridic acid HOPOCl2 and may be obtained by treating POCl3 with water or a lower aliphatic alcohol, e.g. in situ, or by hydrogenation of esters. Excess HCl may be removed during the phosphorylation reaction by passing air or inert gas or by partial neutralization with an organic or inorganic base or a molecular sieve, or a proton acceptor such as an ether may be added. Examples describe the preparation of the sodium salts of 51-inosinic and a guanylic acids and of 21,31 - O - isopropylidene guanosine, inosine, adenosine, cytidine and uridine and 21,31-O-cyclohexylideneinosine. Specification 1,011,994 is referred to.
GB1512263A 1962-04-20 1963-04-17 Processes for the production of 5-ribonucleotides and 2,3-o-alkylidene ribonucleosides Expired GB1013164A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP1537262 1962-04-20
JP3847462 1962-09-10

Publications (1)

Publication Number Publication Date
GB1013164A true GB1013164A (en) 1965-12-15

Family

ID=26351495

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1512263A Expired GB1013164A (en) 1962-04-20 1963-04-17 Processes for the production of 5-ribonucleotides and 2,3-o-alkylidene ribonucleosides

Country Status (2)

Country Link
CH (1) CH420170A (en)
GB (1) GB1013164A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USD384366S (en) 1996-08-08 1997-09-30 Myron Manufacturing Corporation Combination ruler and calculator

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USD384366S (en) 1996-08-08 1997-09-30 Myron Manufacturing Corporation Combination ruler and calculator

Also Published As

Publication number Publication date
CH420170A (en) 1966-09-15

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