KR850007067A - 옥스아자포스포린 유도체의 염의 제조방법 - Google Patents
옥스아자포스포린 유도체의 염의 제조방법 Download PDFInfo
- Publication number
- KR850007067A KR850007067A KR1019850001260A KR850001260A KR850007067A KR 850007067 A KR850007067 A KR 850007067A KR 1019850001260 A KR1019850001260 A KR 1019850001260A KR 850001260 A KR850001260 A KR 850001260A KR 850007067 A KR850007067 A KR 850007067A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- compound
- amino
- general formula
- alkyl
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title claims 7
- ZZVDXRCAGGQFAK-UHFFFAOYSA-N 2h-oxazaphosphinine Chemical class N1OC=CC=P1 ZZVDXRCAGGQFAK-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 150000007514 bases Chemical class 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- BOWUOGIPSRVRSJ-UHFFFAOYSA-N 2-aminohexano-6-lactam Chemical compound NC1CCCCNC1=O BOWUOGIPSRVRSJ-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- FFFHZYDWPBMWHY-VKHMYHEASA-N L-homocysteine Chemical compound OC(=O)[C@@H](N)CCS FFFHZYDWPBMWHY-VKHMYHEASA-N 0.000 claims 3
- -1 benzylthio Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical group 0.000 claims 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical group O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 claims 1
- 108010013381 Porins Proteins 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims 1
- KIWQWJKWBHZMDT-UHFFFAOYSA-N homocysteine thiolactone Chemical compound NC1CCSC1=O KIWQWJKWBHZMDT-UHFFFAOYSA-N 0.000 claims 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 102000007739 porin activity proteins Human genes 0.000 claims 1
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
Classifications
-
- 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
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
- C07F9/65842—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring
- C07F9/65846—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring the phosphorus atom being part of a six-membered ring which may be condensed with another ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (1)
- a) X가 하이드록시그룹 또는 C1-C4-알콕시그룹인 하기 일반식(Ⅲ)의 화합물을,하기 일반식(Ⅳ)의 화합물과 호모시스타인티오릭톤, α-아미노-ε-카프로 락탐 또는 하기 일반식(Ⅱ)의 염기성 화합물과의 염과 반응시키거나, 언급된 일반식(Ⅲ)의 화합물을 우선 하기 일반식(Ⅳ)의 화합물과 반응시키고 이어서 전술된 염기성 화합물과 반응시키거나, X가 벤질티오, C1-C6-알카노일티오, C1-C10-알킬티오, 또는 카복시그룹, 하이드록시그룹 또는 C1-C4-카브알콕시그룹으로 치환된 C1-C10-알킬티오이거나, X가 그룹-N(OH)-CO-NHR[여기서, R은 수소, C1-C6-알킬, 벤질, 페닐, 할로겐-페닐 또는 알킬-페닐이다]이거나, X-가 그룹 A이고 염형태로 존재할 수도 있는 일반식(Ⅲ)의 화합물을 , 과량의 하기 일반식(V)의 화합물, 또는 이의 호모시스타인티오락본 , α-아미노-ε-카프로 락탐 또는 하기 일반식 (Ⅱ)의 염기성 화합물과의 염과 반응시키거나; b) 하기 일반식(Ⅰ)의 화합물 또는 이의 염을 호모시스타인티오락톤, α-아미노-ε-카프로락탐 또는 하기 일반식(Ⅱ)의 화합물과의 염기성 화합물과 반응시켜 상응하는 염을 제조하고, 임의로, 수득된 화합물중의 염기성분, 또는 A가 염형태가 아닌 경우 그룹 A중의 산수소를 하기 기설명 범위내의 다른 염기 성분으로 치환함을 특징으로하는, 하기 일반식(Ⅰ)의 옥스아자포스포린 유도체와 호모시스타인티오릭톤, α-아미노-ε-카프로락탐 또는 하기 일반식(Ⅱ)의 염기성 화학물과 염을 제조방법 :상기식에서, R1, R2및 R3는 동일 또는 상이하며, 수소, 메틸, 에틸, 2-클로로에틸 또는 3-메탄설포닐옥시에틸이고, 이들 잔기중 적어도 2개는 2-클로로에틸 및 /또는 2-메탄설포닐옥시에틸며,A는 그룹-S-alk-SO3H 또는 -N(OH)-CONH-alk-CO2H이고, 여기서, alk는 임의로 머캡토 그룹을 함유하는 C2-C6-알킬렌 잔기이며, alk 그룹에 결합된 카복시그룹이 존재하는 경우 alk는 -CH2-일 수도 있으며, R4는 하이드록시그룹, 아미노그룹 또는 C1-C6-알콕시그룹이고, R5는 수소 또는 디플루오로메틸그룹이며 R6는 수소, 인돌일-(3)-메틸잔기, 이미다졸일-(4)-메틸잔기, C1-C10-알킬그룹; 또는 하이드록시그룹, C1-C6-알콕시그룹, 머캡토그룹, C1-C6-알킬머캡토그룹, 페닐그룹, 하이드록시페닐그룹, 아미노-C1-C6-알킬머캡토그룹, 아미노-C1-C|6-알콕시그룹, 아미노그룹, 아미노카보닐그룹, 우레이도 그룹(H2N CONH-), 구아니디노그룹 또는 C1-C6-알콕시카보닐 그룹으로 치환된 C1-C6-알킬그룹이거나, R6는 결합된 부위>CR5(NR7R8)과 함께 프롤린잔기, 4-하이드록시-프롤린잔기 또는 2-옥소-3아미노-3-디플루오로메틸-피레리딘을 형성하고, R7및 R8은 수소 또는 C1-C6-알킬잔기이며, A´는 A로 정의 된 것과 동일하지만 A와 상이한 것이다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP3407585.2 | 1984-03-01 | ||
DE3407585 | 1984-03-01 | ||
DE3407585.2 | 1984-03-01 | ||
DE3416159.7 | 1984-05-02 | ||
DE3416159 | 1984-05-02 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR850007067A true KR850007067A (ko) | 1985-10-30 |
KR890003789B1 KR890003789B1 (ko) | 1989-10-04 |
Family
ID=25818993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019850001260A KR890003789B1 (ko) | 1984-03-01 | 1985-02-28 | 옥스아자포스포린 유도체의 염의 제조방법 |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0158057B1 (ko) |
KR (1) | KR890003789B1 (ko) |
CA (1) | CA1254903A (ko) |
DE (1) | DE3569737D1 (ko) |
ES (1) | ES8607332A1 (ko) |
FI (1) | FI78705C (ko) |
HU (1) | HUT36829A (ko) |
IE (1) | IE57950B1 (ko) |
IL (1) | IL74473A0 (ko) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1634886A3 (en) * | 1999-03-05 | 2006-03-29 | Metabasis Therapeutics, Inc. | Novel phosphorus-containing prodrug |
ES2272268T3 (es) * | 1999-03-05 | 2007-05-01 | Metabasis Therapeutics, Inc. | Nuevos profarmacos que contienen fosforo. |
US7205404B1 (en) | 1999-03-05 | 2007-04-17 | Metabasis Therapeutics, Inc. | Phosphorus-containing prodrugs |
DE19929021A1 (de) | 1999-06-25 | 2000-12-28 | Degussa | Funktionelle Organylorganyloxysilane auf Trägerstoffen in Kabelcompounds |
EP3623364A1 (en) | 2014-02-13 | 2020-03-18 | Ligand Pharmaceuticals, Inc. | Prodrug compounds and their uses |
CN106687118A (zh) | 2014-07-02 | 2017-05-17 | 配体药物公司 | 前药化合物及其用途 |
JP2021509907A (ja) | 2018-01-09 | 2021-04-08 | リガンド・ファーマシューティカルズ・インコーポレイテッド | アセタール化合物およびその治療的使用 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3133309A1 (de) * | 1980-09-10 | 1982-04-15 | Asta-Werke Ag, Chemische Fabrik, 4800 Bielefeld | 4-carbamoyloxy-oxazaphosphorine, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zubereitungen |
DE3111428A1 (de) * | 1981-03-24 | 1982-10-07 | Asta-Werke Ag, Chemische Fabrik, 4800 Bielefeld | Oxazaphosphorin-4-thio-alkansulfonsaeuren und deren neutrale salze, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zubereitungen |
-
1985
- 1985-02-19 DE DE8585101780T patent/DE3569737D1/de not_active Expired
- 1985-02-19 EP EP85101780A patent/EP0158057B1/de not_active Expired
- 1985-02-27 HU HU85722A patent/HUT36829A/hu unknown
- 1985-02-27 FI FI850800A patent/FI78705C/fi not_active IP Right Cessation
- 1985-02-28 CA CA000475401A patent/CA1254903A/en not_active Expired
- 1985-02-28 ES ES540777A patent/ES8607332A1/es not_active Expired
- 1985-02-28 KR KR1019850001260A patent/KR890003789B1/ko active IP Right Grant
- 1985-02-28 IL IL74473A patent/IL74473A0/xx unknown
- 1985-02-28 IE IE510/85A patent/IE57950B1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
ES540777A0 (es) | 1986-05-16 |
EP0158057B1 (de) | 1989-04-26 |
FI850800A0 (fi) | 1985-02-27 |
IL74473A0 (en) | 1985-05-31 |
FI850800L (fi) | 1985-09-02 |
CA1254903A (en) | 1989-05-30 |
IE850510L (en) | 1985-09-01 |
HUT36829A (en) | 1985-10-28 |
FI78705C (fi) | 1989-09-11 |
EP0158057A1 (de) | 1985-10-16 |
IE57950B1 (en) | 1993-05-19 |
DE3569737D1 (en) | 1989-06-01 |
ES8607332A1 (es) | 1986-05-16 |
FI78705B (fi) | 1989-05-31 |
KR890003789B1 (ko) | 1989-10-04 |
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