DE135371C - - Google Patents
Info
- Publication number
- DE135371C DE135371C DENDAT135371D DE135371DA DE135371C DE 135371 C DE135371 C DE 135371C DE NDAT135371 D DENDAT135371 D DE NDAT135371D DE 135371D A DE135371D A DE 135371DA DE 135371 C DE135371 C DE 135371C
- Authority
- DE
- Germany
- Prior art keywords
- derivatives
- formula
- acetic acid
- new
- alcohol
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000001409 amidines Chemical class 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 claims description 2
- 150000003230 pyrimidines Chemical class 0.000 claims description 2
- 150000002739 metals Chemical group 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- ZXTHWIZHGLNEPG-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC=C1 ZXTHWIZHGLNEPG-UHFFFAOYSA-N 0.000 description 1
- OQLZINXFSUDMHM-UHFFFAOYSA-N Acetamidine Chemical compound CC(N)=N OQLZINXFSUDMHM-UHFFFAOYSA-N 0.000 description 1
- KKSRZRDXERHYFZ-UHFFFAOYSA-N C(C)[Na].C(#N)CC(=O)O Chemical compound C(C)[Na].C(#N)CC(=O)O KKSRZRDXERHYFZ-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 241001072332 Monia Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- PXXJHWLDUBFPOL-UHFFFAOYSA-N benzamidine Chemical compound NC(=N)C1=CC=CC=C1 PXXJHWLDUBFPOL-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- -1 methylene group Metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229940083251 peripheral vasodilators purine derivative Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- KYVISUNMHKSREJ-UHFFFAOYSA-M potassium;2-cyanoacetate Chemical compound [K+].[O-]C(=O)CC#N KYVISUNMHKSREJ-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000000561 purinyl group Chemical class N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 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
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE135371C true DE135371C (enrdf_load_stackoverflow) |
Family
ID=403418
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT135371D Active DE135371C (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE135371C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT135371D patent/DE135371C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1922702A1 (de) | Verfahren zur Herstellung von 1-Glykosyl-5-azacytosinen | |
| DE135371C (enrdf_load_stackoverflow) | ||
| DE1966828C3 (de) | Verfahren zur Herstellung von 3-Pyrazolidinon-Derivaten | |
| DE842065C (de) | Verfahren zur Herstellung stickstoffhaltiger heterocyclischer Verbindungen | |
| DE943706C (de) | Verfahren zur Herstellung von 2, 4-Diamino-5-benzylpyrimidinabkoemmlingen | |
| DE115253C (enrdf_load_stackoverflow) | ||
| DE2065698B2 (de) | Verfahren zur Herstellung von 2-Isopropyl-6-methyl-4(3H)-pyrimidon | |
| DE156384C (enrdf_load_stackoverflow) | ||
| DE838141C (de) | Verfahren zur Herstellung von 2-Chlorpyrimiddn | |
| DE1135913B (de) | Verfahren zur Herstellung von 2-Methyl-4-amino-5-cyanpyrimidin | |
| DE2167194C3 (de) | Verfahren zur Herstellung von 4-Hydroxy-6-chlormethylpyrimidinen | |
| DE937059C (de) | Verfahren zur Herstellung von Aminoderivaten von Polynitroalkoholen | |
| DE756489C (de) | Verfahren zur Herstellung von C-Cycloheptenylbarbitursaeuren | |
| DE1545535A1 (de) | Verfahren zur Herstellung von Inosin und dessen Derivaten | |
| DE156055C (enrdf_load_stackoverflow) | ||
| DE1219489B (de) | Verfahren zur Herstellung von substituierten 5-Thioureidouracilen | |
| DE1200308B (de) | Verfahren zur Herstellung von 4, 6-Dihydroxy-pyrimidinen | |
| DE889151C (de) | Verfahren zur Herstellung von 2, 4-Diamino-5-phenyl-pyrimidin-abkoemmlingen | |
| DE155732C (enrdf_load_stackoverflow) | ||
| DE1695893B1 (de) | Verfahren zur Herstellung von 4-Amino-5-acylamidomethylpyrimidinen | |
| DE1445662C (de) | 4- eckige Klammer auf 2-(5-Nitrofuryl)vinyl eckige Klammer zu -pyrimidine und Verfahren zu ihrer Herstellung | |
| DE2018433C3 (de) | Verfahren zur Herstellung von 2,2disubstituierten 4,5-Imidazolidindionen | |
| AT249048B (de) | Verfahren zur Herstellung von neuen Benzimidazolonderivaten | |
| DE1016266B (de) | Verfahren zur Herstellung von 2-Methyl-4-amino-5-acetaminomethylpyrimidin | |
| DE2944145A1 (de) | Verfahren zur herstellung von 2,4-diaminopyrimidin |