KR850007059A - 페니실린 및 세파로스포린 유도체의 제조방법 - Google Patents
페니실린 및 세파로스포린 유도체의 제조방법 Download PDFInfo
- Publication number
- KR850007059A KR850007059A KR1019840001238A KR840001238A KR850007059A KR 850007059 A KR850007059 A KR 850007059A KR 1019840001238 A KR1019840001238 A KR 1019840001238A KR 840001238 A KR840001238 A KR 840001238A KR 850007059 A KR850007059 A KR 850007059A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- general formula
- organic
- cooh
- reacting
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 5
- 229930186147 Cephalosporin Chemical class 0.000 title claims 2
- 229930182555 Penicillin Natural products 0.000 title claims 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical class N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 title claims 2
- 229940124587 cephalosporin Drugs 0.000 title claims 2
- 150000001780 cephalosporins Chemical class 0.000 title claims 2
- 229940049954 penicillin Drugs 0.000 title claims 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 2
- 150000007530 organic bases Chemical class 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims 1
- -1 3,4-dihydroxyphenyl Chemical group 0.000 claims 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 1
- 239000004472 Lysine Substances 0.000 claims 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims 1
- 238000005917 acylation reaction Methods 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000003840 hydrochlorides Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000005545 phthalimidyl group Chemical group 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000004434 sulfur atom Chemical group 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cephalosporin Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (4)
- 일반식(Ⅱ)의 유기산과 일반식(Ⅲ)의 아실화제를 유기염기 존재하여 유기용매 중에서 반응시켜 얻은 반응성 에스테르를 일반식(V)의 6-아미노페니실란산 유도체나 7-아미노세파로스포란산 유도체의 염산염과 반응시키는 일반식(Ⅰ)의 페니실린 및 세파로스포린 유도체의 제조방법.상기 식에서, R은 페닐, 4-히드록시페닐, 3,4-디하드록시페닐, 1-히드록시에틸기이며, R2는 수소또는 메톡시기이고, R3는 -(CH3)2-CH(COOH)- 또는 -CH2C(CH2R3)=C(COOH)-기이다.(여기서 R3는 1개 또는 2이상의 질소나 1개의 황원자를 함유하고 또한 저급알킬기로 치환되어 있어도 좋은 5원 복소환기이다). R4는 벤조트리아졸릴, 피리딜기, 썩신신이미딜, 프탈이미딜기이거, n는 1또는 2이다.
- 제 1항에 있어서, 유기용매를 N,N-디메틸포름아미드, N,N-디메틸아세트아미드 또는 N-메틸-2-피롤리돈 중에서 선택하는 제조방법.
- 제 1항에 있어서, 아실화반응을 실온에서 2-5시간 범위에서 행하는 제조방법.
- 제 1항에 유기염기를 피리딘, 트리에틸아민, N,N-디메틸아미노피리딘 중에서 선택하는 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019840001238A KR860001086B1 (ko) | 1984-03-12 | 1984-03-12 | 페니실린 및 세파로스포린 유도체의 제조방법 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019840001238A KR860001086B1 (ko) | 1984-03-12 | 1984-03-12 | 페니실린 및 세파로스포린 유도체의 제조방법 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR850007059A true KR850007059A (ko) | 1985-10-30 |
| KR860001086B1 KR860001086B1 (ko) | 1986-08-07 |
Family
ID=19233154
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019840001238A KR860001086B1 (ko) | 1984-03-12 | 1984-03-12 | 페니실린 및 세파로스포린 유도체의 제조방법 |
Country Status (1)
| Country | Link |
|---|---|
| KR (1) | KR860001086B1 (ko) |
-
1984
- 1984-03-12 KR KR1019840001238A patent/KR860001086B1/ko active Pre-grant Review Request
Also Published As
| Publication number | Publication date |
|---|---|
| KR860001086B1 (ko) | 1986-08-07 |
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| Date | Code | Title | Description |
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| G160 | Decision to publish patent application | ||
| O035 | Opposition [patent]: request for opposition |
Free format text: OPPOSITION NUMBER: 001986001230; OPPOSITION DATE: 19861007 |