DE163200A - - Google Patents
Info
- Publication number
- DE163200A DE163200A DE163200A DE 163200 A DE163200 A DE 163200A DE 163200 A DE163200 A DE 163200A
- Authority
- DE
- Germany
- Prior art keywords
- acid
- thiourea
- guanidine
- dissolved
- dialkylmalonamic
- 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.)
- Pending
Links
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 11
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 10
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 5
- 239000004202 carbamide Substances 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 4
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 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 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- -1 diethylmalonamic acid ester Chemical class 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- FTOAOBMCPZCFFF-UHFFFAOYSA-N 5,5-diethylbarbituric acid Chemical compound CCC1(CC)C(=O)NC(=O)NC1=O FTOAOBMCPZCFFF-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 229960002319 barbital Drugs 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- IGRWHBBHXVNZEO-UHFFFAOYSA-N guanidine;hypochlorous acid Chemical compound ClO.NC(N)=N IGRWHBBHXVNZEO-UHFFFAOYSA-N 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
- 239000000203 mixture Substances 0.000 description 1
- RCOUWKSZRXJXLA-UHFFFAOYSA-N propylbarbital Chemical compound CCCC1(CCC)C(=O)NC(=O)NC1=O RCOUWKSZRXJXLA-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1620694C3 (de) | Verfahren zur Herstellung von 5-Methyl-7-diäthylamino-s-triazolo [1,5-a] pyrimidin und seinen Salzen mit Säuren | |
DE163200A (enrdf_load_stackoverflow) | ||
DE2652004C3 (de) | l-Acyl-2-arylamino-2-imidazoline, Verfahren zu ihrer Herstellung und ihre Verwendung | |
DE2166270C3 (de) | Nicotinoylaminoäthansulfonyl-2amino-thiazol | |
DE597305C (de) | Verfahren zur Herstellung von aliphatischen primaeren Aminosaeuren oder deren Derivaten | |
DE943706C (de) | Verfahren zur Herstellung von 2, 4-Diamino-5-benzylpyrimidinabkoemmlingen | |
DE624230C (de) | Verfahren zur Herstellung von Glutamin | |
DE158592C (enrdf_load_stackoverflow) | ||
DE180291C (enrdf_load_stackoverflow) | ||
DE335993C (de) | Verfahren zur Herstellung von Hydantoinen | |
DE2065698B2 (de) | Verfahren zur Herstellung von 2-Isopropyl-6-methyl-4(3H)-pyrimidon | |
DE572204C (de) | Verfahren zur Herstellung von Aminoaethansulfonsaeuren | |
DE170657C (enrdf_load_stackoverflow) | ||
DE172980C (enrdf_load_stackoverflow) | ||
DE134984C (enrdf_load_stackoverflow) | ||
DE156384C (enrdf_load_stackoverflow) | ||
DE1237560B (de) | Verfahren zur Herstellung von Cyanameisensaeurethiolestern | |
DE145604C (enrdf_load_stackoverflow) | ||
DE1593832C3 (de) | Verfahren zur Herstellung von Calcium DL Pantothenat | |
DE756489C (de) | Verfahren zur Herstellung von C-Cycloheptenylbarbitursaeuren | |
DE386743C (de) | Verfahren zur Darstellung von N-Alkylaminofettsaeuren und deren N-Acidylderivaten | |
AT346848B (de) | Verfahren zur herstellung von 2,4-diamino-5-(2- methyl-4,5-dimethoxybenzyl)-pyrimidin | |
DE2429781C2 (de) | Verfahren zur Herstellung von N,N-Bis-(2-cyanoäthyl)-amino-phenolen | |
DE845516C (de) | Verfahren zur Darstellung von primaeren aliphatischen, aromatischaliphatischen bzw. cycloaliphatischen Aminen | |
DE473519C (de) | Verfahren zur Darstellung von Ureiden |