NO743491L - - Google Patents
Info
- Publication number
- NO743491L NO743491L NO743491A NO743491A NO743491L NO 743491 L NO743491 L NO 743491L NO 743491 A NO743491 A NO 743491A NO 743491 A NO743491 A NO 743491A NO 743491 L NO743491 L NO 743491L
- Authority
- NO
- Norway
- Prior art keywords
- methylene
- deoxy
- minutes
- demethyl
- tetracyclines
- Prior art date
Links
- 239000004098 Tetracycline Substances 0.000 claims description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
- 229940040944 tetracyclines Drugs 0.000 claims description 8
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical group C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- OUULRIDHGPHMNQ-UHFFFAOYSA-N stibane Chemical group [SbH3] OUULRIDHGPHMNQ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical group [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 claims description 3
- 238000005695 dehalogenation reaction Methods 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 150000003003 phosphines Chemical group 0.000 claims description 2
- 230000002829 reductive effect Effects 0.000 claims description 2
- 229960002180 tetracycline Drugs 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 239000002798 polar solvent Substances 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 10
- 235000019364 tetracycline Nutrition 0.000 description 5
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910000074 antimony hydride Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000003522 tetracyclines Chemical class 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- -1 organic acid salts Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229960004368 oxytetracycline hydrochloride Drugs 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000006894 reductive elimination reaction Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2948873 | 1973-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO743491L true NO743491L (ja) | 1975-04-28 |
Family
ID=11227078
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO743491A NO743491L (ja) | 1973-09-28 | 1974-09-26 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US3962330A (ja) |
| JP (1) | JPS5062969A (ja) |
| AT (1) | AT337893B (ja) |
| AU (1) | AU7381574A (ja) |
| BE (1) | BE820475A (ja) |
| CA (1) | CA1118770A (ja) |
| DE (1) | DE2446588A1 (ja) |
| DK (1) | DK501474A (ja) |
| ES (1) | ES430510A1 (ja) |
| FR (1) | FR2246537B1 (ja) |
| IL (1) | IL45740A0 (ja) |
| NL (1) | NL7412763A (ja) |
| NO (1) | NO743491L (ja) |
| SE (1) | SE7412217L (ja) |
| ZA (1) | ZA746121B (ja) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4987242A (en) * | 1988-10-28 | 1991-01-22 | Jagmohan Khanna | Hydrogenation catalyst useful in the production of alpha-6-deoxytetracyclines |
| KR101336462B1 (ko) * | 2004-05-21 | 2013-12-04 | 프레지던트 앤드 펠로우즈 오브 하바드 칼리지 | 테트라사이클린 및 이의 유사체의 합성 |
| EP2016044B1 (en) * | 2006-04-07 | 2020-06-10 | President and Fellows of Harvard College | Pentacycline derivatives for the treatment of infections |
| EP2487160B1 (en) * | 2006-10-11 | 2016-02-03 | President and Fellows of Harvard College | Synthesis of Enone Intermediate |
| EP2424834B1 (en) | 2009-04-30 | 2018-07-11 | President and Fellows of Harvard College | Synthesis of tetracyclines and intermediates thereof |
| CN107827823B (zh) * | 2017-11-22 | 2020-01-31 | 大连奇凯医药科技有限公司 | 4,5-二溴咪唑的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3250809A (en) * | 1962-09-06 | 1966-05-10 | Pfizer & Co C | 6-deoxy-6-demethyl-6-halomethylene tetracyclines and their 11a-chloro and fluoro derivatives |
| US3649700A (en) * | 1966-12-20 | 1972-03-14 | Knapsack Ag | Process for the dehydrochlorination of chlorinated hydrocarbons |
| US3659006A (en) * | 1969-06-17 | 1972-04-25 | Borg Warner | Synthesis of alpha-haloacrylonitrile |
-
1974
- 1974-09-24 US US05/509,054 patent/US3962330A/en not_active Expired - Lifetime
- 1974-09-24 DK DK501474A patent/DK501474A/da not_active Application Discontinuation
- 1974-09-25 CA CA000210078A patent/CA1118770A/en not_active Expired
- 1974-09-25 IL IL45740A patent/IL45740A0/xx unknown
- 1974-09-26 NO NO743491A patent/NO743491L/no unknown
- 1974-09-26 ZA ZA00746121A patent/ZA746121B/xx unknown
- 1974-09-26 AT AT776474A patent/AT337893B/de not_active IP Right Cessation
- 1974-09-27 SE SE7412217A patent/SE7412217L/xx unknown
- 1974-09-27 BE BE149014A patent/BE820475A/xx unknown
- 1974-09-27 NL NL7412763A patent/NL7412763A/xx unknown
- 1974-09-28 JP JP49112211A patent/JPS5062969A/ja active Pending
- 1974-09-28 ES ES430510A patent/ES430510A1/es not_active Expired
- 1974-09-30 AU AU73815/74A patent/AU7381574A/en not_active Expired
- 1974-09-30 FR FR7432898A patent/FR2246537B1/fr not_active Expired
- 1974-09-30 DE DE19742446588 patent/DE2446588A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR2246537B1 (ja) | 1978-08-11 |
| JPS5062969A (ja) | 1975-05-29 |
| IL45740A0 (en) | 1974-11-29 |
| AU7381574A (en) | 1976-04-01 |
| AT337893B (de) | 1977-07-25 |
| SE7412217L (ja) | 1975-04-01 |
| NL7412763A (nl) | 1975-04-02 |
| DE2446588A1 (de) | 1975-04-03 |
| BE820475A (fr) | 1975-01-16 |
| CA1118770A (en) | 1982-02-23 |
| ATA776474A (de) | 1976-11-15 |
| ES430510A1 (es) | 1976-10-01 |
| FR2246537A1 (ja) | 1975-05-02 |
| US3962330A (en) | 1976-06-08 |
| ZA746121B (en) | 1975-11-26 |
| DK501474A (ja) | 1975-05-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO743491L (ja) | ||
| US3663562A (en) | Process for the production of 2-mercapto-benzothiazole | |
| US3257460A (en) | Preparation of tertiary phosphines | |
| EP4140992A1 (en) | Method for preparing s-nicotine | |
| US3429903A (en) | Method of preparing molybdenum (iii) acetylacetonate | |
| KR20190061478A (ko) | 리튬 플루오로술포닐이미드의 제조방법 및 이를 이용한 리튬 플루오로술포닐이미드 | |
| JPS5945666B2 (ja) | アミノカルボン酸類の製造方法 | |
| SU1690543A3 (ru) | Способ получени производных пиридин-2,3-дикарбоновых кислот или их N-окисей | |
| US4045494A (en) | Method for preparing triogranophosphines | |
| US4249023A (en) | Process for manufacturing triphenylphosphine | |
| EP0010368B1 (en) | Process for production of benzene phosphonic dihalide | |
| EP0101625B1 (en) | Process for preparing the 2',4'-difluoro-4-hydroxy-(1,1'-diphenyl)-3-carboxylic acid | |
| US4248845A (en) | Process for preparing crystalline phosphonitrilic chloride oligomers | |
| US6133447A (en) | Process for the preparation of substituted pyridines | |
| CN112961092B (zh) | 一种富马酸沃诺拉赞中间体的制备方法 | |
| US3313821A (en) | Process for preparing pyridine carboxylic acids from compounds having a pyridine nucleus | |
| EP1810975A1 (en) | Method for producing phosphonate having alcoholic hydroxy group | |
| EP0525038A1 (en) | PROCESS FOR THE PREPARATION OF BIS (DIHYDROXYETHYL) ETHER OF RESORCINOL. | |
| JPH05202058A (ja) | ５，６，１１，１２−テトラチオテトラセンの製造方法 | |
| US4388251A (en) | Method for preparing 2-chlorobenzoyl chloride | |
| US3597440A (en) | Salts of isoperthiocyanic acid | |
| KR820000327B1 (ko) | 메틸 에페드린 염산염의 제법 | |
| JPH0481576B2 (ja) | ||
| KR910002281B1 (ko) | 베타-레조시놀산의 제조방법 | |
| US2872485A (en) | Process |