ATE42299T1 - Verfahren zur herstellung von n(dibenzyloxyphosphoryl)-cyanamid und die verfahren, die solche verbindungen als zwischenprodukt fuer die synthese von phosphagenstoffen verwenden. - Google Patents
Verfahren zur herstellung von n(dibenzyloxyphosphoryl)-cyanamid und die verfahren, die solche verbindungen als zwischenprodukt fuer die synthese von phosphagenstoffen verwenden.Info
- Publication number
- ATE42299T1 ATE42299T1 AT85200080T AT85200080T ATE42299T1 AT E42299 T1 ATE42299 T1 AT E42299T1 AT 85200080 T AT85200080 T AT 85200080T AT 85200080 T AT85200080 T AT 85200080T AT E42299 T1 ATE42299 T1 AT E42299T1
- Authority
- AT
- Austria
- Prior art keywords
- dibenzyloxyphosphoryl
- compounds
- processes
- cyanamide
- synthesis
- Prior art date
Links
- DRBBFCLWYRJSJZ-UHFFFAOYSA-N N-phosphocreatine Chemical compound OC(=O)CN(C)C(=N)NP(O)(O)=O DRBBFCLWYRJSJZ-UHFFFAOYSA-N 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 3
- 230000015572 biosynthetic process Effects 0.000 title abstract 2
- 239000000126 substance Substances 0.000 title abstract 2
- 238000003786 synthesis reaction Methods 0.000 title abstract 2
- -1 DIBENZYLOXYPHOSPHORYL Chemical class 0.000 title 1
- 238000002360 preparation method Methods 0.000 title 1
- JHJRGYVXKRRRIU-UHFFFAOYSA-N 2-[[(e)-n'-bis(phenylmethoxy)phosphorylcarbamimidoyl]-methylamino]acetic acid Chemical compound C=1C=CC=CC=1COP(=O)(N=C(N)N(CC(O)=O)C)OCC1=CC=CC=C1 JHJRGYVXKRRRIU-UHFFFAOYSA-N 0.000 abstract 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 abstract 1
- YADJFRGSGWGMNH-UHFFFAOYSA-N [chloro(phenylmethoxy)phosphoryl]oxymethylbenzene Chemical compound C=1C=CC=CC=1COP(=O)(Cl)OCC1=CC=CC=C1 YADJFRGSGWGMNH-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- NTOFBGNUFLRFBO-UHFFFAOYSA-N bis(phenylmethoxy)phosphorylcyanamide Chemical compound C=1C=CC=CC=1COP(NC#N)(=O)OCC1=CC=CC=C1 NTOFBGNUFLRFBO-UHFFFAOYSA-N 0.000 abstract 1
- 229940109239 creatinine Drugs 0.000 abstract 1
- HIPLEPXPNLWKCQ-UHFFFAOYSA-N fosfocreatinine Chemical compound CN1CC(=O)N=C1NP(O)(O)=O HIPLEPXPNLWKCQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229950007002 phosphocreatine Drugs 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical class C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2479—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2458—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic of aliphatic amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT19426/84A IT1173206B (it) | 1984-02-02 | 1984-02-02 | Procedimento per la preparazione di n-(dibenzilossifosforil) cianammide,composto cosi' ottenuto,processi che utilizzano detto composto quale intermedio di sintesi di sostanze fosfagene e sostanze in tal modo prodotte |
| EP85200080A EP0150883B1 (de) | 1984-02-02 | 1985-01-25 | Verfahren zur Herstellung von N-(Dibenzyloxyphosphoryl)-cyanamid und die Verfahren, die solche Verbindungen als Zwischenprodukt für die Synthese von Phosphagenstoffen verwenden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE42299T1 true ATE42299T1 (de) | 1989-05-15 |
Family
ID=11157803
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT85200080T ATE42299T1 (de) | 1984-02-02 | 1985-01-25 | Verfahren zur herstellung von n(dibenzyloxyphosphoryl)-cyanamid und die verfahren, die solche verbindungen als zwischenprodukt fuer die synthese von phosphagenstoffen verwenden. |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0150883B1 (de) |
| AT (1) | ATE42299T1 (de) |
| DE (1) | DE3569531D1 (de) |
| IT (1) | IT1173206B (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102153587B (zh) * | 2011-03-07 | 2013-01-23 | 南京亚东启天药业有限公司 | 一种二苄氧基磷酰肌酐的合成方法 |
| IT201800003896A1 (it) | 2018-03-27 | 2019-09-27 | Alfasigma Spa | Composizione acquosa stabile di fosfocreatina. |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH401989A (fr) * | 1958-09-26 | 1965-11-15 | Kuhlmann Ets | Procédé de préparation de la phosphocréatine |
| DE1905362A1 (de) * | 1969-02-04 | 1970-09-17 | Bayer Ag | Phosphor-,Phosphon- bzw.Thiono-phosphor-(phosphon)saeureester und Verfahren zu ihrer Herstellung |
-
1984
- 1984-02-02 IT IT19426/84A patent/IT1173206B/it active
-
1985
- 1985-01-25 DE DE8585200080T patent/DE3569531D1/de not_active Expired
- 1985-01-25 AT AT85200080T patent/ATE42299T1/de not_active IP Right Cessation
- 1985-01-25 EP EP85200080A patent/EP0150883B1/de not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IT8419426A0 (it) | 1984-02-02 |
| EP0150883A2 (de) | 1985-08-07 |
| EP0150883B1 (de) | 1989-04-19 |
| IT1173206B (it) | 1987-06-18 |
| DE3569531D1 (en) | 1989-05-24 |
| EP0150883A3 (en) | 1985-08-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| UEP | Publication of translation of european patent specification | ||
| EELA | Cancelled due to lapse of time |