PL69908B1 - - Google Patents
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- Publication number
- PL69908B1 PL69908B1 PL1966137020A PL13702066A PL69908B1 PL 69908 B1 PL69908 B1 PL 69908B1 PL 1966137020 A PL1966137020 A PL 1966137020A PL 13702066 A PL13702066 A PL 13702066A PL 69908 B1 PL69908 B1 PL 69908B1
- Authority
- PL
- Poland
- Prior art keywords
- formula
- carbon atoms
- general formula
- aldehyde
- alkyl radical
- Prior art date
Links
- 239000002253 acid Substances 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 150000002825 nitriles Chemical class 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical group 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 102100035861 Cytosolic 5'-nucleotidase 1A Human genes 0.000 claims 4
- 101000802744 Homo sapiens Cytosolic 5'-nucleotidase 1A Proteins 0.000 claims 4
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
- 230000000844 anti-bacterial effect Effects 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- OPHQOIGEOHXOGX-UHFFFAOYSA-N 3,4,5-trimethoxybenzaldehyde Chemical compound COC1=CC(C=O)=CC(OC)=C1OC OPHQOIGEOHXOGX-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
- -1 alkyl radical Chemical class 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- HUPVIAINOSTNBJ-HWKANZROSA-N (e)-3-ethoxyprop-2-enenitrile Chemical compound CCO\C=C\C#N HUPVIAINOSTNBJ-HWKANZROSA-N 0.000 description 1
- RVBFWXYFXKDVKG-UHFFFAOYSA-N 2-ethoxyprop-2-enenitrile Chemical compound CCOC(=C)C#N RVBFWXYFXKDVKG-UHFFFAOYSA-N 0.000 description 1
- DAUAQNGYDSHRET-UHFFFAOYSA-N 3,4-dimethoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1OC DAUAQNGYDSHRET-UHFFFAOYSA-N 0.000 description 1
- XHPZVBGIPQQTQW-UHFFFAOYSA-N 5-benzylpyrimidine-2,4-diamine Chemical class NC1=NC(N)=NC=C1CC1=CC=CC=C1 XHPZVBGIPQQTQW-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- GPVDHNVGGIAOQT-UHFFFAOYSA-N Veratric acid Natural products COC1=CC=C(C(O)=O)C(OC)=C1 GPVDHNVGGIAOQT-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- LNDJVIYUJOJFSO-UHFFFAOYSA-N cyanoacetylene Chemical group C#CC#N LNDJVIYUJOJFSO-UHFFFAOYSA-N 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
- YWOITFUKFOYODT-UHFFFAOYSA-N methanol;sodium Chemical compound [Na].OC YWOITFUKFOYODT-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000004954 trialkylamino group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
- C07D239/49—Two nitrogen atoms with an aralkyl radical, or substituted aralkyl radical, attached in position 5, e.g. trimethoprim
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Jib Cranes (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB45657/65A GB1142654A (en) | 1965-10-28 | 1965-10-28 | Cyano-acetals and their use in benzylpyrimidine synthesis |
Publications (1)
Publication Number | Publication Date |
---|---|
PL69908B1 true PL69908B1 (en, 2012) | 1973-10-31 |
Family
ID=10438067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1966137020A PL69908B1 (en, 2012) | 1965-10-28 | 1966-10-27 |
Country Status (16)
Country | Link |
---|---|
US (2) | US3513185A (en, 2012) |
JP (1) | JPS50657B1 (en, 2012) |
AT (1) | AT271479B (en, 2012) |
BE (1) | BE689071A (en, 2012) |
BR (1) | BR6684142D0 (en, 2012) |
CH (1) | CH484875A (en, 2012) |
DE (2) | DE1793767C3 (en, 2012) |
DK (3) | DK120546B (en, 2012) |
ES (1) | ES332806A1 (en, 2012) |
FI (1) | FI49716C (en, 2012) |
GB (1) | GB1142654A (en, 2012) |
IL (1) | IL26755A (en, 2012) |
NL (1) | NL150442B (en, 2012) |
NO (1) | NO127616B (en, 2012) |
PL (1) | PL69908B1 (en, 2012) |
SE (3) | SE390634B (en, 2012) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1261455A (en) * | 1969-03-06 | 1972-01-26 | Burroughs Wellcome Co | Improvements in or relating to substituted acrylonitriles |
DE2065367C2 (de) * | 1969-03-06 | 1985-04-04 | The Wellcome Foundation Ltd., London | Verfahren zur Herstellung von 2,4- Diamino-5-benzylpyrimidinen |
BE789904A (fr) * | 1971-10-12 | 1973-04-10 | Wellcome Found | Procedes de synthese organique |
USRE29467E (en) * | 1971-12-20 | 1977-11-08 | Plantex, Ltd. | Benzylcyano-amides |
US3910984A (en) * | 1972-11-27 | 1975-10-07 | Plantex Ltd | Benzylcyano-amides |
AR207561A1 (es) * | 1973-03-17 | 1976-10-15 | Heumann Ludwig & Co Gmbh | Procedimiento para la sintesis de 2,4-diamino 5(3'-metoxi-5'-substituido o no-4'alquildioxial-quilen-bencil)pirimidina |
DK397574A (en, 2012) * | 1973-08-24 | 1975-04-28 | Ciba Geigy Ag | |
US4515948A (en) * | 1973-09-12 | 1985-05-07 | Hoffmann-La Roche Inc. | 2,4-Diamino-5-(4-amino and 4-dimethylamino-3,5-dimethoxy benzyl)pyrimidines |
DE2623170C2 (de) * | 1976-05-22 | 1982-03-11 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von α-Cyanzimtaldehyd-Derivaten und 3,4,5-Trimethoxy-α-Cyanzimtaldehyd |
GB1582245A (en) * | 1976-06-09 | 1981-01-07 | Wellcome Found | Benzyl cyanoacetal derivatives and their conversion to pyrimidine derivatives |
US4659861A (en) * | 1981-11-03 | 1987-04-21 | The Dow Chemical Company | Novel nitrile functional glycol ether acetals |
DE3211679A1 (de) * | 1982-03-30 | 1983-10-06 | Dynamit Nobel Ag | Verfahren zur herstellung von acetalen und enolaethern aus acyloxymethylenverbindungen |
JPS59120U (ja) * | 1982-06-22 | 1984-01-05 | 株式会社タカハベッド | 歩行練習器を兼ねた身障者用椅子 |
FR2602507B1 (fr) * | 1986-08-08 | 1989-06-09 | Sanofi Pharma | Procede de preparation de diamino-2,4 benzyl-5 pyrimidines |
CA2095518A1 (en) * | 1990-11-14 | 1992-05-15 | Jeffrey M. Blaney | Specific inhibition of dihydrofolate reductase and compounds therefor |
CN103570631B (zh) * | 2013-11-21 | 2016-05-25 | 华中农业大学 | 氚标记二甲氧苄啶的制备方法 |
CN103601688A (zh) * | 2013-11-25 | 2014-02-26 | 四川大学 | 一种甲氧苄啶杂质的合成方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2755298A (en) * | 1956-07-17 | pwiiq | ||
US3049544A (en) * | 1962-08-14 | Method for the preparation of | ||
US2745866A (en) * | 1953-01-22 | 1956-05-15 | Searle & Co | Alpha, beta-diaryl substitution products of alpha-alkenonitriles |
US2951089A (en) * | 1953-12-28 | 1960-08-30 | Schering Corp | Alkyl ethers of polyiodophenyl propionic acids |
US3128300A (en) * | 1960-12-09 | 1964-04-07 | Monsanto Chemicals | 3-phenoxyacrylonitriles prepared by cyanovinylation reaction |
US3485840A (en) * | 1964-11-12 | 1969-12-23 | Hoffmann La Roche | 2,4-diamino - 5 - (2',4',5'-substituted benzyl) pyrimidines,intermediates and processes |
-
1965
- 1965-10-28 GB GB45657/65A patent/GB1142654A/en not_active Expired
-
1966
- 1966-10-18 US US587392A patent/US3513185A/en not_active Expired - Lifetime
- 1966-10-24 DK DK552966AA patent/DK120546B/da unknown
- 1966-10-25 IL IL26755A patent/IL26755A/xx unknown
- 1966-10-25 NO NO00165336A patent/NO127616B/no unknown
- 1966-10-26 DE DE1793767A patent/DE1793767C3/de not_active Expired
- 1966-10-26 CH CH1551866A patent/CH484875A/de not_active IP Right Cessation
- 1966-10-26 DE DE1593723A patent/DE1593723C3/de not_active Expired
- 1966-10-27 FI FI662845A patent/FI49716C/fi active
- 1966-10-27 PL PL1966137020A patent/PL69908B1/pl unknown
- 1966-10-27 BR BR184142/66A patent/BR6684142D0/pt unknown
- 1966-10-27 ES ES0332806A patent/ES332806A1/es not_active Expired
- 1966-10-28 SE SE7206667*3A patent/SE390634B/xx unknown
- 1966-10-28 AT AT1003066A patent/AT271479B/de active
- 1966-10-28 NL NL666615287A patent/NL150442B/xx not_active IP Right Cessation
- 1966-10-28 SE SE12357/69A patent/SE349580B/xx unknown
- 1966-10-28 SE SE14832/66A patent/SE344746B/xx unknown
- 1966-10-28 BE BE689071D patent/BE689071A/xx not_active IP Right Cessation
-
1968
- 1968-12-13 JP JP43091040A patent/JPS50657B1/ja active Pending
-
1969
- 1969-05-23 DK DK281669AA patent/DK127415B/da unknown
- 1969-06-12 US US832830A patent/US3671564A/en not_active Expired - Lifetime
-
1970
- 1970-08-19 DK DK425970AA patent/DK125849B/da unknown
Also Published As
Publication number | Publication date |
---|---|
FI49716B (en, 2012) | 1975-06-02 |
AT271479B (de) | 1969-06-10 |
JPS50657B1 (en, 2012) | 1975-01-10 |
DE1793767B2 (de) | 1979-10-31 |
NO127616B (en, 2012) | 1973-07-23 |
DE1793767C3 (de) | 1980-07-10 |
DE1593723B2 (de) | 1977-06-16 |
NL6615287A (en, 2012) | 1967-05-02 |
DK125849B (da) | 1973-05-14 |
IL26755A (en) | 1970-10-30 |
DK127415B (da) | 1973-11-05 |
DK120546B (da) | 1971-06-14 |
BR6684142D0 (pt) | 1973-12-26 |
CH484875A (de) | 1970-01-31 |
US3671564A (en) | 1972-06-20 |
GB1142654A (en) | 1969-02-12 |
SE390634B (sv) | 1977-01-03 |
BE689071A (en, 2012) | 1967-04-28 |
SE349580B (en, 2012) | 1972-10-02 |
NL150442B (nl) | 1976-08-16 |
DE1593723A1 (de) | 1972-04-13 |
FI49716C (fi) | 1975-09-10 |
SE344746B (en, 2012) | 1972-05-02 |
US3513185A (en) | 1970-05-19 |
DE1793767A1 (de) | 1973-11-08 |
DE1593723C3 (de) | 1978-04-27 |
ES332806A1 (es) | 1967-10-01 |
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