KR900009658A - 아실화 방법 - Google Patents
아실화 방법 Download PDFInfo
- Publication number
- KR900009658A KR900009658A KR1019890019012A KR890019012A KR900009658A KR 900009658 A KR900009658 A KR 900009658A KR 1019890019012 A KR1019890019012 A KR 1019890019012A KR 890019012 A KR890019012 A KR 890019012A KR 900009658 A KR900009658 A KR 900009658A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- compound
- mixed
- amino
- pyridinium
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 8
- 230000010933 acylation Effects 0.000 title 1
- 238000005917 acylation reaction Methods 0.000 title 1
- 150000008064 anhydrides Chemical class 0.000 claims 4
- -1 amino pyridinium compound Chemical class 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000005059 halophenyl group Chemical group 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 2
- 125000003944 tolyl group Chemical group 0.000 claims 2
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- PFZCOWLKXHIVII-UHFFFAOYSA-N pyridin-1-ium-1-amine Chemical compound N[N+]1=CC=CC=C1 PFZCOWLKXHIVII-UHFFFAOYSA-N 0.000 claims 1
- 150000003512 tertiary amines Chemical class 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
- C07D501/38—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
- C07D501/46—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- 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
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
- C07F9/6539—Five-membered rings
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)
- Cephalosporin Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (8)
- 약 -15℃ 내지 약 20℃의 불활성 유기 용매에서 하기 일반식(IB)의 혼합된 무수물을 하기 구조식(IA)의 아미노 피리디늄 화합물과 혼합함을 포함하는 하기구조식(Ⅰ)화합물의 제조방법 :상기식에서, R은 일반식 -SO2R1(이때, R1은 C1-C4알킬, 페닐, 메틸페닐, 할로페닐 또는 나프틸이다)의 설포닐 그룹이거나, 또는 -P(O)(OR2)2(이때, R2는 C1-C4알킬, 페닐, 메틸페닐 또는 할로페닐이다)의 포스페이트 에스테르 그룹이다.
- 제1항에 있어서, 상기 아미노 피리디늄 핵 화합물을, 3급 아민 존재하에 혼합된 무수물과 혼합하는 방법.
- 제2항에 있어서, 상기 불활성 유기 용매가 DMF 또는 DMAC 인 방법.
- 제1항에 있어서, 상기 아미노-피리디늄 핵 화합물이 트리알킬 실릴화된 유도체 형태인 방법.
- 제4항에 있어서, 상기 실릴화된 유도체가 트리메틸실릴화된 유도체인 방법.
- 제1항에 있어서, 상기 혼합된 무수물의 R이 설포닐 그룹 -SO2R1인 방법.
- 제6항에 있어서, R1이 메틸 또는 에틸인 방법.
- 제1항에 있어서, 상기 혼합된 무수물의 R이 그룹 -P(O)(OR2)2인 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019980014866A KR0180907B1 (ko) | 1988-12-27 | 1998-04-25 | 설폰산 또는 인산의 혼합 무수물 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29068088A | 1988-12-27 | 1988-12-27 | |
US07/290,680 | 1988-12-27 | ||
US7/290,680 | 1988-12-27 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019980014866A Division KR0180907B1 (ko) | 1988-12-27 | 1998-04-25 | 설폰산 또는 인산의 혼합 무수물 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR900009658A true KR900009658A (ko) | 1990-07-05 |
KR0159760B1 KR0159760B1 (ko) | 1998-12-01 |
Family
ID=23117097
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890019012A KR0159760B1 (ko) | 1988-12-27 | 1989-12-20 | 아실화 방법 |
KR1019980014866A KR0180907B1 (ko) | 1988-12-27 | 1998-04-25 | 설폰산 또는 인산의 혼합 무수물 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019980014866A KR0180907B1 (ko) | 1988-12-27 | 1998-04-25 | 설폰산 또는 인산의 혼합 무수물 |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0377987A3 (ko) |
JP (1) | JP3068143B2 (ko) |
KR (2) | KR0159760B1 (ko) |
CA (1) | CA2006341A1 (ko) |
IL (1) | IL92810A (ko) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR950013578B1 (ko) * | 1993-04-10 | 1995-11-09 | 주식회사럭키 | 신규 티아(디아)졸 초산의 반응성 티오포스페이트 유도체 및 그의 제조방법 |
EP0791597B1 (en) * | 1996-02-21 | 2000-07-12 | Lupin Laboratories Limited | Method for manufacture of cephalosporins and intermediates thereof |
EP0791596A1 (en) * | 1996-02-21 | 1997-08-27 | Lupin Laboratories Limited | Method for manufacture of cephalosporins and intermediates thereof |
US5831085A (en) * | 1997-01-16 | 1998-11-03 | Lupin Laboratories Limited | Process for manufacture of cephalosporin such as ceftazidime and intermediate thereof |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR228726A1 (es) * | 1978-05-26 | 1983-04-15 | Glaxo Group Ltd | Procedimiento para la preparacion del antibiotico(6r,7r)-7-((z)-2-(2-aminotiazol-4-il)-2-(2-carboxiprop-2-oxiimino)acetamido)-3-(1-piridiniometil)cef-3-em-4-carboxilato |
FR2439785A1 (fr) * | 1978-10-23 | 1980-05-23 | Roussel Uclaf | Nouveau procede de preparation des produits derives de l'acide 7-amino-thiazolyl acetamido cephalosporanique |
FR2462439A1 (fr) * | 1979-07-26 | 1981-02-13 | Roussel Uclaf | Nouveau procede de preparation de produits derives de l'acide 7-/(2-aryl) 2-hydroxyimino acetamido/cephalosporanique |
DE3419015A1 (de) * | 1984-05-22 | 1985-11-28 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von cephalosporinen |
DE3542644A1 (de) * | 1985-12-03 | 1987-06-04 | Hoechst Ag | Verfahren zur herstellung von cefodizim |
-
1989
- 1989-12-20 EP EP19890313373 patent/EP0377987A3/en not_active Withdrawn
- 1989-12-20 IL IL9281089A patent/IL92810A/en unknown
- 1989-12-20 KR KR1019890019012A patent/KR0159760B1/ko not_active IP Right Cessation
- 1989-12-21 CA CA002006341A patent/CA2006341A1/en not_active Abandoned
- 1989-12-22 JP JP1334678A patent/JP3068143B2/ja not_active Expired - Lifetime
-
1998
- 1998-04-25 KR KR1019980014866A patent/KR0180907B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CA2006341A1 (en) | 1990-06-27 |
IL92810A (en) | 1994-12-29 |
JPH02215786A (ja) | 1990-08-28 |
JP3068143B2 (ja) | 2000-07-24 |
KR0180907B1 (ko) | 1999-10-01 |
KR0159760B1 (ko) | 1998-12-01 |
EP0377987A2 (en) | 1990-07-18 |
EP0377987A3 (en) | 1991-08-28 |
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A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
LAPS | Lapse due to unpaid annual fee |