KR880001688A - 피리미딘과 푸린염기의 n-포스포닐메톡시 알킬유도체와 그의 제조 방법 - Google Patents
피리미딘과 푸린염기의 n-포스포닐메톡시 알킬유도체와 그의 제조 방법 Download PDFInfo
- Publication number
- KR880001688A KR880001688A KR1019870007844A KR870007844A KR880001688A KR 880001688 A KR880001688 A KR 880001688A KR 1019870007844 A KR1019870007844 A KR 1019870007844A KR 870007844 A KR870007844 A KR 870007844A KR 880001688 A KR880001688 A KR 880001688A
- Authority
- KR
- South Korea
- Prior art keywords
- pyrimidine
- purine base
- following general
- general formula
- residue
- Prior art date
Links
- 102000004961 Furin Human genes 0.000 title claims 2
- 108090001126 Furin Proteins 0.000 title claims 2
- 125000000217 alkyl group Chemical group 0.000 title claims 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 claims abstract 12
- 150000001875 compounds Chemical class 0.000 claims abstract 7
- 230000000840 anti-viral effect Effects 0.000 claims abstract 3
- 238000006243 chemical reaction Methods 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims abstract 2
- 150000003230 pyrimidines Chemical class 0.000 claims abstract 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 9
- -1 amine salt Chemical class 0.000 claims 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 4
- 229910052783 alkali metal Inorganic materials 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 150000001340 alkali metals Chemical class 0.000 claims 2
- 229910021529 ammonia Inorganic materials 0.000 claims 2
- 150000005690 diesters Chemical class 0.000 claims 2
- 229930024421 Adenine Natural products 0.000 claims 1
- 229960000643 adenine Drugs 0.000 claims 1
- GFFGJBXGBJISGV-UHFFFAOYSA-N adenyl group Chemical group N1=CN=C2N=CNC2=C1N GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 claims 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- 239000002585 base Substances 0.000 claims 1
- FZXSSJIKXCFPDP-UHFFFAOYSA-N chloro(dichlorophosphoryl)methane Chemical compound ClCP(Cl)(Cl)=O FZXSSJIKXCFPDP-UHFFFAOYSA-N 0.000 claims 1
- 238000006317 isomerization reaction Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000003729 nucleotide group Chemical group 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
- C07F9/65616—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (4)
- 다음 일반식(I)로 표시되는 피리미딘과 푸린염기의 N-포스포닐메톡시알킬유도체.(윗식에서, R은 수소원자 또느 하이드록시메틸기이며, B는 피리미딘 또는 푸린염기의 잔기 (비치환 아데닌잔기는 제외), 알칼리금속, 암모니아 또는 아민염이다.)
- 다음 일반식(II)로 표시되는 화합물과 R-톨루엔설포닐메탄포스핀산의 디에스테르를 먼저 반응시키고, 이어서 트리메틸할로게노실란과 반응시키거나 또는,B-CH2CH2OH..............................(II)(윗식에서, B는 피리미딘 또는 푸린 염기의 잔기이다.)피리미딘이나 푸린염기의 알카리금속염과 다음 일반식(III)으로 표시되는 2-브로모에톡시메탄포스핀산의 디에스테르를 반응시켜서BrCH2CH2OCH2P(O)(OC2H5)2...................(III)다음 일반식(IV)로 표시된느 중간체화합물을 생성시킨 다음,B-CH2CH2OCH2P(O)(OC2H5)2..........................(IV)(윗식에서, B는 피리미딘 또는 푸린염기의 잔기이다.)이를 트리메틸할로게노실란으로 처리시켜서 되어짐을 특징으로 하는 다음 일반식(I)로 표시되는 피리미딘과 푸린염기의 N-포스포닐메톡시알킬유도체의 제조 방법.(윗식에서, R은 수소원자이고, B는 피리미딘 또는 푸린염기의 잔기이다.)
- 다음 일반식(V)로 표시되는 화합물과,B-CH2CH(OH)CH2OH..................................(V)(윗식에서, B는 피리미딘 또는 푸린염기의 잔기이다.)다음 일반식(VI)로 표시되는 크로로메탄 포스포닐 디클로라이드와 반응시켜서 얻어진 에스테르화합물을,CICH2P(O)Cl2.............................(VI)다음 일반식(VII)로 표시되는 에스테르화합물로이성질체화시킨 다음에 이들을 수용성알카리 금속수산화물로 처리시켜서 되어짐을 특징으로 하는 다음식(I)로 표시되는 피리미딘과 푸린염기의 N-포스포닐메톡시 알킬유도체의 제조 방법.(윗식에서, R은 히드록시메틸기이고, B는 피리미딘 또는 푸린염기의 잔기이다.)
- 항바이러스활성을 가지며 다음 일반식(I)로 표시되는 화합물을 함유하고 있는 것을 특징으로 하는 치료학적 조성물(윗식에서, R은 수소원자 또는 히드록시메틸기이고, B는 활성성분인 피리미딘 또는 푸린염기의 유기잔기이거나 알카리금속, 암모니아 또는 아민염이다)※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CZPV5469-86 | 1986-07-18 | ||
CS865469A CS264222B1 (en) | 1986-07-18 | 1986-07-18 | N-phosphonylmethoxyalkylderivatives of bases of pytimidine and purine and method of use them |
Publications (2)
Publication Number | Publication Date |
---|---|
KR880001688A true KR880001688A (ko) | 1988-04-26 |
KR950004179B1 KR950004179B1 (en) | 1995-04-27 |
Family
ID=5399635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR87007844A KR950004179B1 (en) | 1986-07-18 | 1987-07-18 | N-phosphonylmethoxyalkye derivatives of pyrimidine and purine bases and a therapeutical composition therefrom with antiviral activity |
Country Status (21)
Country | Link |
---|---|
US (3) | US5142051A (ko) |
EP (1) | EP0253412B1 (ko) |
JP (1) | JPH0822866B2 (ko) |
KR (1) | KR950004179B1 (ko) |
AT (1) | ATE57932T1 (ko) |
AU (1) | AU600002B2 (ko) |
CA (1) | CA1340856C (ko) |
CS (1) | CS264222B1 (ko) |
DE (2) | DE19775085I2 (ko) |
DK (1) | DK170646B1 (ko) |
EG (1) | EG18273A (ko) |
ES (1) | ES2036194T3 (ko) |
FI (1) | FI86856C (ko) |
GR (1) | GR3002534T3 (ko) |
IE (1) | IE60117B1 (ko) |
IL (1) | IL83235A (ko) |
LU (1) | LU90155I2 (ko) |
NL (1) | NL970036I2 (ko) |
NZ (1) | NZ221100A (ko) |
PT (1) | PT85354B (ko) |
ZA (1) | ZA875283B (ko) |
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AU521577B2 (en) * | 1977-02-24 | 1982-04-22 | Wellcome Foundation Limited, The | 9-hydroxyethoxymethyl guanine phosphates |
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1986
- 1986-07-18 CS CS865469A patent/CS264222B1/cs not_active IP Right Cessation
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1987
- 1987-07-16 NZ NZ221100A patent/NZ221100A/xx unknown
- 1987-07-17 ZA ZA875283A patent/ZA875283B/xx unknown
- 1987-07-17 DE DE1997175085 patent/DE19775085I2/de active Active
- 1987-07-17 ES ES198787110399T patent/ES2036194T3/es not_active Expired - Lifetime
- 1987-07-17 CA CA000542404A patent/CA1340856C/en not_active Expired - Lifetime
- 1987-07-17 DK DK373487A patent/DK170646B1/da not_active IP Right Cessation
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- 1987-07-17 EP EP87110399A patent/EP0253412B1/en not_active Expired - Lifetime
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- 1987-07-17 IE IE194487A patent/IE60117B1/en not_active IP Right Cessation
- 1987-07-17 AT AT87110399T patent/ATE57932T1/de active
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- 1987-07-18 KR KR87007844A patent/KR950004179B1/ko not_active IP Right Cessation
- 1987-07-19 EG EG42/87A patent/EG18273A/xx active
- 1987-07-20 PT PT85354A patent/PT85354B/pt unknown
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1990
- 1990-11-19 GR GR90400937T patent/GR3002534T3/el unknown
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1994
- 1994-10-11 US US08/320,591 patent/US5641763A/en not_active Expired - Lifetime
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1995
- 1995-03-28 US US08/412,398 patent/US5869467A/en not_active Expired - Lifetime
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1997
- 1997-10-01 NL NL970036C patent/NL970036I2/nl unknown
- 1997-10-21 LU LU90155C patent/LU90155I2/fr unknown
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