AT207042B - Process for the production of pharmaceutical preparations which contain purines and / or purine derivatives - Google Patents
Process for the production of pharmaceutical preparations which contain purines and / or purine derivativesInfo
- Publication number
- AT207042B AT207042B AT323857A AT323857A AT207042B AT 207042 B AT207042 B AT 207042B AT 323857 A AT323857 A AT 323857A AT 323857 A AT323857 A AT 323857A AT 207042 B AT207042 B AT 207042B
- Authority
- AT
- Austria
- Prior art keywords
- production
- pharmaceutical preparations
- purine derivatives
- purines
- sep
- Prior art date
Links
- 150000003212 purines Chemical class 0.000 title claims description 6
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 238000000034 method Methods 0.000 title claims description 3
- 229940083251 peripheral vasodilators purine derivative Drugs 0.000 title claims description 3
- 239000000825 pharmaceutical preparation Substances 0.000 title claims description 3
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 claims description 6
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 claims description 6
- 229960000278 theophylline Drugs 0.000 claims description 5
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 claims description 4
- 229960004559 theobromine Drugs 0.000 claims description 4
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 claims description 3
- 229960001948 caffeine Drugs 0.000 claims description 3
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 claims description 3
- 239000002126 C01EB10 - Adenosine Substances 0.000 claims description 2
- 229960005305 adenosine Drugs 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 2
- YAPQBXQYLJRXSA-UHFFFAOYSA-N theobromine Chemical compound CN1C(=O)NC(=O)C2=C1N=CN2C YAPQBXQYLJRXSA-UHFFFAOYSA-N 0.000 claims 2
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 claims 1
- 229930024421 Adenine Natural products 0.000 claims 1
- 229960000643 adenine Drugs 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- -1 salts purines Chemical class 0.000 claims 1
- 239000000829 suppository Substances 0.000 claims 1
- 239000003826 tablet Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 2
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Herstellung von pharmazeutischen Präparaten, die Purine und bzw. oder Purinderivate enthalten
EMI1.1
EMI1.2
<tb>
<tb> wasserlöslichenWasserlöslichkeit <SEP> in <SEP> So <SEP>
<tb> Theophyllin <SEP> 0, <SEP> 5 <SEP>
<tb> Coffein <SEP> 1, <SEP> 5 <SEP>
<tb> Adenosin <SEP> 0, <SEP> 5 <SEP>
<tb> 7- <SEP> (6 <SEP> -Aminoäthyl) <SEP> -theophyllin <SEP> über <SEP> 50
<tb> 1- <SEP> (ss-Äthylaminoäthyl)-theobromin. <SEP> HCI <SEP> über <SEP> 50
<tb> 1- <SEP> (8 <SEP> -Diäthylaminoäthyl) <SEP> -theobrominrhodanid <SEP> über <SEP> 18. <SEP>
<tb>
<Desc/Clms Page number 2>
Beispiel 1: 5,6g 7-(ss-Aminoäthyl)-theophyllin werden mit 5, 0 g Theophyllin und zu 100 g Lösung mit Wasser vermischt. Es entsteht eine stabile Lösung.
Beispiel 2: 10,0 g 1-(ss-Diäthylaminoäthyl)-theobrominrhodanid werden mit 5, 0 g Coffein und zu 100 g Lösung mit Wasser vermischt. Es entsteht eine stabile Lösung.
EMI2.1
3 : 30, 0g l- (ss-Äthylaminoäthyl)-theobromir. HCJ werdenzu 100 g Lösung mit Wasser vermischt. Es entsteht eine stabile Lösung.
<Desc / Clms Page number 1>
Process for the production of pharmaceutical preparations which contain purines and / or purine derivatives
EMI1.1
EMI1.2
<tb>
<tb> water soluble water solubility <SEP> in <SEP> So <SEP>
<tb> Theophylline <SEP> 0, <SEP> 5 <SEP>
<tb> Caffeine <SEP> 1, <SEP> 5 <SEP>
<tb> Adenosine <SEP> 0, <SEP> 5 <SEP>
<tb> 7- <SEP> (6 <SEP> -aminoethyl) <SEP> -theophylline <SEP> over <SEP> 50
<tb> 1- <SEP> (ss-ethylaminoethyl) -theobromine. <SEP> HCI <SEP> via <SEP> 50
<tb> 1- <SEP> (8 <SEP> -Diethylaminoäthyl) <SEP> -theobromine rhodanide <SEP> via <SEP> 18. <SEP>
<tb>
<Desc / Clms Page number 2>
Example 1: 5.6 g of 7- (ss-aminoethyl) -theophylline are mixed with 5.0 g of theophylline and 100 g of solution with water. A stable solution is created.
Example 2: 10.0 g of 1- (ss-diethylaminoethyl) -theobromine rhodanide are mixed with 5.0 g of caffeine and 100 g of solution with water. A stable solution is created.
EMI2.1
3:30, 0g l- (ss-ethylaminoethyl) -theobromir. HCJ are mixed with water to make 100 g of the solution. A stable solution is created.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE207042X | 1956-05-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT207042B true AT207042B (en) | 1960-01-11 |
Family
ID=5793496
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT323857A AT207042B (en) | 1956-05-17 | 1957-05-16 | Process for the production of pharmaceutical preparations which contain purines and / or purine derivatives |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT207042B (en) |
-
1957
- 1957-05-16 AT AT323857A patent/AT207042B/en active
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