PL434722A1 - Heksahydroimidazo[1',2':3,4]imidazo[1,2-a]pirazyno-5,10(4aH,6H)-dion i 3,8-difenylo-1,4,7,10-tetraazacyklododeka-3,7-dieno-2,9-dion oraz sposób ich wytwarzania - Google Patents
Heksahydroimidazo[1',2':3,4]imidazo[1,2-a]pirazyno-5,10(4aH,6H)-dion i 3,8-difenylo-1,4,7,10-tetraazacyklododeka-3,7-dieno-2,9-dion oraz sposób ich wytwarzaniaInfo
- Publication number
- PL434722A1 PL434722A1 PL434722A PL43472220A PL434722A1 PL 434722 A1 PL434722 A1 PL 434722A1 PL 434722 A PL434722 A PL 434722A PL 43472220 A PL43472220 A PL 43472220A PL 434722 A1 PL434722 A1 PL 434722A1
- Authority
- PL
- Poland
- Prior art keywords
- dione
- hexahydroimidazo
- imidazo
- pyrazine
- diphenyl
- Prior art date
Links
- UBJMJNGLLVVQEQ-UHFFFAOYSA-N N1CCN2C1C(N1C2C(NCC1)=O)=O Chemical compound N1CCN2C1C(N1C2C(NCC1)=O)=O UBJMJNGLLVVQEQ-UHFFFAOYSA-N 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- TYEYBOSBBBHJIV-UHFFFAOYSA-M 2-oxobutanoate Chemical compound CCC(=O)C([O-])=O TYEYBOSBBBHJIV-UHFFFAOYSA-M 0.000 abstract 1
- UHXKPSNPCCTHGM-UHFFFAOYSA-N C1(=CC=CC=C1)C=1C(NCCNC(C(=NCCN=1)C1=CC=CC=C1)=O)=O Chemical compound C1(=CC=CC=C1)C=1C(NCCNC(C(=NCCN=1)C1=CC=CC=C1)=O)=O UHXKPSNPCCTHGM-UHFFFAOYSA-N 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 238000004440 column chromatography Methods 0.000 abstract 1
- QKLCQKPAECHXCQ-UHFFFAOYSA-N ethyl phenylglyoxylate Chemical compound CCOC(=O)C(=O)C1=CC=CC=C1 QKLCQKPAECHXCQ-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Przedmiotem wynalazku jest heksahydroimidazo[1',2':3,4]imidazo[1,2-a]pirazyno-5,10(4aH,6H)-dion o wzorze 1 lub 3,8-difenylo-1,4,7,10-tetraazacyklododeka-3,7-dieno-2,9-dion o wzorze 2. Zgłoszenie obejmuje także sposób wytwarzania heksahydroimidazo[1',2',:3,4]imidazo[1,2]pirazyno-5,10(4aH,6H)-dionu o wzorze 1 lub 3,8-difenylo-1,4,7,10-tetraazacyklododeka-3,7-dieno-2,9-dionu o wzorze 2 polega na tym, że etylenodiaminę poddaje się reakcji z glioksalanem etylu lub benzoilomrówczanem etylu, po czym produkt oczyszcza się na drodze chromatografii kolumnowej.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL434722A PL434722A1 (pl) | 2020-07-20 | 2020-07-20 | Heksahydroimidazo[1',2':3,4]imidazo[1,2-a]pirazyno-5,10(4aH,6H)-dion i 3,8-difenylo-1,4,7,10-tetraazacyklododeka-3,7-dieno-2,9-dion oraz sposób ich wytwarzania |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL434722A PL434722A1 (pl) | 2020-07-20 | 2020-07-20 | Heksahydroimidazo[1',2':3,4]imidazo[1,2-a]pirazyno-5,10(4aH,6H)-dion i 3,8-difenylo-1,4,7,10-tetraazacyklododeka-3,7-dieno-2,9-dion oraz sposób ich wytwarzania |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL434722A1 true PL434722A1 (pl) | 2022-01-24 |
Family
ID=80111538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL434722A PL434722A1 (pl) | 2020-07-20 | 2020-07-20 | Heksahydroimidazo[1',2':3,4]imidazo[1,2-a]pirazyno-5,10(4aH,6H)-dion i 3,8-difenylo-1,4,7,10-tetraazacyklododeka-3,7-dieno-2,9-dion oraz sposób ich wytwarzania |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL434722A1 (pl) |
-
2020
- 2020-07-20 PL PL434722A patent/PL434722A1/pl unknown
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