PL55785B1 - - Google Patents
Download PDFInfo
- Publication number
- PL55785B1 PL55785B1 PL108648A PL10864865A PL55785B1 PL 55785 B1 PL55785 B1 PL 55785B1 PL 108648 A PL108648 A PL 108648A PL 10864865 A PL10864865 A PL 10864865A PL 55785 B1 PL55785 B1 PL 55785B1
- Authority
- PL
- Poland
- Prior art keywords
- formula
- acid addition
- addition salt
- nitrate
- reacted
- Prior art date
Links
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims 7
- 239000002253 acid Substances 0.000 claims 6
- 238000000034 method Methods 0.000 claims 5
- 239000012458 free base Substances 0.000 claims 2
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical class NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- SDDKIZNHOCEXTF-UHFFFAOYSA-N methyl carbamimidothioate Chemical compound CSC(N)=N SDDKIZNHOCEXTF-UHFFFAOYSA-N 0.000 claims 1
- ZODDGFAZWTZOSI-UHFFFAOYSA-N nitric acid;sulfuric acid Chemical compound O[N+]([O-])=O.OS(O)(=O)=O ZODDGFAZWTZOSI-UHFFFAOYSA-N 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- -1 sulfate nitrate nitrate nitrate nitrate nitrate Chemical compound 0.000 description 2
- YKIOKAURTKXMSB-UHFFFAOYSA-N adams's catalyst Chemical compound O=[Pt]=O YKIOKAURTKXMSB-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL55785B1 true PL55785B1 (cs) | 1968-06-25 |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4001212A (en) | Macrocyclic polyamines | |
| AT394725B (de) | Verfahren zur herstellung von neuen mitomycin-c-analogen | |
| ES8204997A1 (es) | Un procedimiento para la preparacion de derivados de cefa- losporina | |
| ES482918A1 (es) | Procedimiento para la preparacion de derivados de indanilo | |
| DE3475302D1 (en) | Carbacyclins, process for their manufacture and their use as pharmaceutical compounds | |
| GB1120463A (en) | Derivatives of 1,3-diazafluoranthene-1-oxide | |
| CH614448A5 (en) | Process for the preparation of novel tertiary amines and their acid addition salts, and compounds thus prepared | |
| GB1567958A (en) | Piperazine and piperazine homologue derivatives and preparation and use thereof | |
| PL55785B1 (cs) | ||
| Osdene et al. | Pteridinecarboxamide Diuretics. II. Reaction of 4, 6-Diamino-5-nitrosopyrimidines with N-Substituted Cyanoacetamides | |
| GB1077151A (en) | Novel dibenzocycloheptatriene derivatives and a process for their manufacture | |
| CH534687A (de) | Verfahren zur Herstellung von Derivaten des 2-Oxo-1,2-dihydro-chinolins | |
| DE2114884A1 (de) | Basisch substituierte Derivate des 1(2H)-Phthalazinons | |
| der Manin-Luther-Universitit | SYNTHESIS OF N-SUBSTITUTED 2, CDIAMINOTHIAZOLES AND THEIR SALTS | |
| CY1585A (en) | Pyrroloindole derivatives | |
| IE771700L (en) | C3-carboxamido derivatives of vinblastine alkaloids | |
| DE836937C (de) | Verfahren zur Herstellung von Piperazoniumverbindungen | |
| GB1128052A (en) | Alkanolamine derivatives | |
| SE8300432D0 (sv) | Reaktiva kanelsyraderivat for framstellning av biologiskt aktiva amider | |
| SU1109396A1 (ru) | Способ получени замещенных пергидро-1,2,4,5-дитиадиазин-1,1,4,4-тетроксидов | |
| FI66355C (fi) | Foerfarande foer framstaellning av 2-isopropylaminopyrimidin | |
| GB1598630A (en) | N-cyano-n'-alkynyl-n''-(2-mercaptoethyl)-guanidines | |
| EP0091576A3 (en) | 7-oxo-4-thia-1-azabicyclo(3,2,0)heptane derivatives | |
| DE2333014A1 (de) | Neue immoniumsalze, verfahren zu ihrer herstellung und ihre anwendung bei der organischen synthese | |
| ES451375A1 (es) | Procedimiento para la preparacion de 2-4 diamino-5-bencil-pirimidinas. |