DD274223A5 - Verfahren zur herstellung von macrolidverbindungen - Google Patents

Verfahren zur herstellung von macrolidverbindungen Download PDF

Info

Publication number: DD274223A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; compound; compounds; group; carried out
Prior art date: 1987-09-11

Application number

DD88319662A

Other languages

German (de)

English (en)

Inventor

Stephan Freeman

Original Assignee

American Cyanamid Company,Us

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.)

1987-09-11

Filing date

1988-09-09

Publication date

1989-12-13

1988-09-09 Application filed by American Cyanamid Company,Us filed Critical American Cyanamid Company,Us

1989-12-13 Publication of DD274223A5 publication Critical patent/DD274223A5/de

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 27
239000003120 macrolide antibiotic agent Substances 0.000 title abstract description 3
238000004519 manufacturing process Methods 0.000 title abstract 2
238000000034 method Methods 0.000 claims abstract description 14
229910052799 carbon Inorganic materials 0.000 claims abstract description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 6
239000003444 phase transfer catalyst Substances 0.000 claims abstract description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 4
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims abstract description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 3
125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
238000006243 chemical reaction Methods 0.000 claims description 6
150000002148 esters Chemical class 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
239000002253 acid Substances 0.000 claims description 4
229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
239000011707 mineral Substances 0.000 claims description 4
239000007800 oxidant agent Substances 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 3
239000011734 sodium Substances 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
150000005621 tetraalkylammonium salts Chemical group 0.000 claims description 2
DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical group CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 4
241000607479 Yersinia pestis Species 0.000 abstract description 3
238000003898 horticulture Methods 0.000 abstract description 3
244000045947 parasite Species 0.000 abstract description 3
238000003860 storage Methods 0.000 abstract description 3
239000003814 drug Substances 0.000 abstract description 2
230000015572 biosynthetic process Effects 0.000 abstract 1
230000001590 oxidative effect Effects 0.000 abstract 1
238000003786 synthesis reaction Methods 0.000 abstract 1
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
238000000855 fermentation Methods 0.000 description 8
230000004151 fermentation Effects 0.000 description 8
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
238000006640 acetylation reaction Methods 0.000 description 6
-1 For example Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
230000021736 acetylation Effects 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 3
239000002054 inoculum Substances 0.000 description 3
239000002609 medium Substances 0.000 description 3
235000010755 mineral Nutrition 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
241000187747 Streptomyces Species 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
150000001721 carbon Chemical group 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
238000010828 elution Methods 0.000 description 2
238000002955 isolation Methods 0.000 description 2
244000005700 microbiome Species 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
238000003756 stirring Methods 0.000 description 2
JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
241000242583 Scyphozoa Species 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
239000012346 acetyl chloride Substances 0.000 description 1
239000012345 acetylating agent Substances 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
230000001178 anti-ectoparasitic effect Effects 0.000 description 1
230000001679 anti-nematodal effect Effects 0.000 description 1
239000012431 aqueous reaction media Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
150000001718 carbodiimides Chemical class 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
230000020176 deacylation Effects 0.000 description 1
238000005947 deacylation reaction Methods 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
238000009826 distribution Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000001640 fractional crystallisation Methods 0.000 description 1
238000005194 fractionation Methods 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical class C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
238000000622 liquid--liquid extraction Methods 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000000203 mixture Substances 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
239000012071 phase Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
150000003566 thiocarboxylic acids Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/22—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains four or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/01—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing oxygen

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Molecular Biology (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
Biotechnology (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Saccharide Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Steroid Compounds (AREA)

DD88319662A 1987-09-11 1988-09-09 Verfahren zur herstellung von macrolidverbindungen DD274223A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB878721374A GB8721374D0 (en)	1987-09-11	1987-09-11	Chemical process

Publications (1)

Publication Number	Publication Date
DD274223A5 true DD274223A5 (de)	1989-12-13

Family

ID=10623611

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD88319662A DD274223A5 (de)	1987-09-11	1988-09-09	Verfahren zur herstellung von macrolidverbindungen

Country Status (13)

Country	Link
EP (1)	EP0307222A3 (da)
JP (1)	JP2635121B2 (da)
KR (1)	KR960010792B1 (da)
AU (1)	AU621064B2 (da)
BR (1)	BR8804665A (da)
CA (1)	CA1339131C (da)
DD (1)	DD274223A5 (da)
DK (1)	DK167683B1 (da)
GB (1)	GB8721374D0 (da)
HU (1)	HU202236B (da)
NZ (1)	NZ226120A (da)
PT (1)	PT88467B (da)
ZA (1)	ZA886740B (da)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR102453881B1 (ko) *	2020-12-29	2022-10-12	주식회사 더블유에스지	베벨링 효율이 향상된 스테인리스 스틸 튜브의 가공방법
KR102453873B1 (ko) *	2020-12-29	2022-10-12	주식회사 더블유에스지	열처리 특성이 우수한 강관의 제조방법, 이에 의해 제조되는 강관

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES2051731T3 (es) *	1986-01-23	1994-07-01	American Cyanamid Co	Un procedimiento para preparar antibioticos macrolidos y su uso.
EP0259779B1 (en) *	1986-09-12	1994-08-10	American Cyanamid Company	23-Oxo (Keto) and 23-imino Derivatives of LL-F28249 Compounds

1987
- 1987-09-11 GB GB878721374A patent/GB8721374D0/en active Pending
1988
- 1988-09-09 NZ NZ226120A patent/NZ226120A/en unknown
- 1988-09-09 CA CA000576929A patent/CA1339131C/en not_active Expired - Fee Related
- 1988-09-09 JP JP63224829A patent/JP2635121B2/ja not_active Expired - Lifetime
- 1988-09-09 BR BR8804665A patent/BR8804665A/pt not_active IP Right Cessation
- 1988-09-09 HU HU884655A patent/HU202236B/hu not_active IP Right Cessation
- 1988-09-09 DK DK504988A patent/DK167683B1/da active
- 1988-09-09 AU AU22092/88A patent/AU621064B2/en not_active Ceased
- 1988-09-09 ZA ZA886740A patent/ZA886740B/xx unknown
- 1988-09-09 PT PT88467A patent/PT88467B/pt not_active IP Right Cessation
- 1988-09-09 KR KR1019880011659A patent/KR960010792B1/ko not_active Expired - Fee Related
- 1988-09-09 EP EP88308346A patent/EP0307222A3/en not_active Withdrawn
- 1988-09-09 DD DD88319662A patent/DD274223A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
KR890005117A (ko)	1989-05-11
JPH01156992A (ja)	1989-06-20
EP0307222A3 (en)	1989-10-18
HU202236B (en)	1991-02-28
GB8721374D0 (en)	1987-10-21
DK504988D0 (da)	1988-09-09
AU2209288A (en)	1989-03-16
AU621064B2 (en)	1992-03-05
EP0307222A2 (en)	1989-03-15
HUT48254A (en)	1989-05-29
JP2635121B2 (ja)	1997-07-30
ZA886740B (en)	1989-08-30
BR8804665A (pt)	1989-04-18
PT88467B (pt)	1992-11-30
NZ226120A (en)	1990-01-29
PT88467A (pt)	1988-10-01
DK167683B1 (da)	1993-12-06
KR960010792B1 (ko)	1996-08-08
DK504988A (da)	1989-03-12
CA1339131C (en)	1997-07-29

Legal Events

Date	Code	Title	Description
2000-02-17	ENJ	Ceased due to non-payment of renewal fee

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DE69409360T2 (de)	1998-07-23	Neue antiparasitische mittel, derivate von milbemycin und avermectin
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EP0216731B1 (de)	1990-03-14	Makrozyklische Antibiotika
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DE2302935A1 (de)	1973-08-02	Semi-synthetische antibiotika mit makrocyclischer lactonstruktur
DE3044970C2 (da)	1988-06-30
DE2559913C2 (de)	1984-02-09	Verfahren zur Herstellung von Cephalosporinderivaten
KR960010792B1 (ko)	1996-08-08	마크롤리드 화합물의 제조 방법
DD274224A5 (de)	1989-12-13	Verfahren zur herstellung von macrolidverbindungen
US4281170A (en)	1981-07-28	Process for the preparation of pyrethrins and analogues thereof and insecticidal compositions containing the same
DE69313871T2 (de)	1998-01-08	Antiparasitisches mittel
DE3134596A1 (de)	1982-08-19	Carbamatderivate, insektizide, antimilben- oder nematozide zusammensetzungen, welche diese enthalten, und verfahren zu deren herstellung
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DD274420A5 (de)	1989-12-20	Verfahren zur herstellung von macrolidverbindungen
DD253822A5 (de)	1988-02-03	Verfahren zur herstellung eines neuen, als mittel gegen parasiten geeigneten avermectin-derivates
DD140047A5 (de)	1980-02-06	Verfahren zur herstellung racemischer und optisch aktiver halbprostanoid-glycoside und-thioglycoside
DE1953338B2 (de)	1975-09-25	Acylderivate des Antibiotikums T-2636C und Verfahren zu ihrer Herstellung sowie diese enthaltende pharmazeutische Mittel
DE1620591A1 (de)	1970-05-14	Cyclische Lincomycincarbonat- und -thiocarbonatester und Verfahren zu ihrer Herstellung
DE2230729B2 (de)	1974-06-20	Verfahren zur Herstellung von Monoestern des Makrolidantibioticums SF-837
DE2445195B2 (de)	1976-11-11	9-0-acyl-3''-0-acyloxymethylderivate des antibioticums sf-837 sowie verfahren zur herstellung derselben