GB913931A - Iminopyrrolines - Google Patents
IminopyrrolinesInfo
- Publication number
- GB913931A GB913931A GB710559A GB710559A GB913931A GB 913931 A GB913931 A GB 913931A GB 710559 A GB710559 A GB 710559A GB 710559 A GB710559 A GB 710559A GB 913931 A GB913931 A GB 913931A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- hydrogen
- pyrroline
- trimethyl
- saturated aliphatic
- 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.)
- Expired
Links
- ZEXGMSRTZFKOQY-UHFFFAOYSA-N N=C1CNC=C1 Chemical class N=C1CNC=C1 ZEXGMSRTZFKOQY-UHFFFAOYSA-N 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000001931 aliphatic group Chemical class 0.000 abstract 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- OXLZQDIFPSMHMX-UHFFFAOYSA-N 3,3,5-trimethyl-N-octadecyl-1H-pyrrol-2-imine Chemical compound CC=1NC(C(C1)(C)C)=NCCCCCCCCCCCCCCCCCC OXLZQDIFPSMHMX-UHFFFAOYSA-N 0.000 abstract 1
- SFFQPNJKUYISKC-UHFFFAOYSA-N 3,3,5-trimethyl-N-phenylpyrrol-2-amine Chemical compound CC=1NC(C(C1)(C)C)=NC1=CC=CC=C1 SFFQPNJKUYISKC-UHFFFAOYSA-N 0.000 abstract 1
- BOITUCPLZUMDTJ-UHFFFAOYSA-N CC=1NC(C(C1)(C)C)=NC Chemical compound CC=1NC(C(C1)(C)C)=NC BOITUCPLZUMDTJ-UHFFFAOYSA-N 0.000 abstract 1
- 101100037762 Caenorhabditis elegans rnh-2 gene Proteins 0.000 abstract 1
- VQMGUYQGNBLITF-UHFFFAOYSA-N N-benzyl-3,3,5-trimethyl-1H-pyrrol-2-imine Chemical compound CC=1NC(C(C1)(C)C)=NCC1=CC=CC=C1 VQMGUYQGNBLITF-UHFFFAOYSA-N 0.000 abstract 1
- LTSLFHHESAOAKV-UHFFFAOYSA-N N-butyl-3,3,5-trimethyl-1H-pyrrol-2-imine Chemical compound CC=1NC(C(C1)(C)C)=NCCCC LTSLFHHESAOAKV-UHFFFAOYSA-N 0.000 abstract 1
- WLOATVQRTNRBGO-UHFFFAOYSA-N N-dodecyl-3,3,5-trimethyl-1H-pyrrol-2-imine Chemical compound CC=1NC(C(C1)(C)C)=NCCCCCCCCCCCC WLOATVQRTNRBGO-UHFFFAOYSA-N 0.000 abstract 1
- DKPONTSSLJMVTE-UHFFFAOYSA-N N-dodecyl-5-methyl-1,3-dihydropyrrol-2-imine Chemical compound CC=1NC(CC1)=NCCCCCCCCCCCC DKPONTSSLJMVTE-UHFFFAOYSA-N 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 238000007080 aromatic substitution reaction Methods 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- GTBRTGPZZALPNS-MXHVRSFHSA-N cyanoketone Chemical compound C1C=C2C(C)(C)C(=O)[C@H](C#N)C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@](C)(O)[C@@]1(C)CC2 GTBRTGPZZALPNS-MXHVRSFHSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- JSGHQDAEHDRLOI-UHFFFAOYSA-N oxomalononitrile Chemical class N#CC(=O)C#N JSGHQDAEHDRLOI-UHFFFAOYSA-N 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/40—Nitrogen atoms, not forming part of a nitro radical, e.g. isatin semicarbazone
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/96—Spiro-condensed ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71850158A | 1958-03-03 | 1958-03-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB913931A true GB913931A (en) | 1962-12-28 |
Family
ID=24886305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB710559A Expired GB913931A (en) | 1958-03-03 | 1959-03-02 | Iminopyrrolines |
Country Status (3)
| Country | Link |
|---|---|
| DE (1) | DE1175238B (enrdf_load_stackoverflow) |
| GB (1) | GB913931A (enrdf_load_stackoverflow) |
| NL (1) | NL236636A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3984563A (en) * | 1973-09-10 | 1976-10-05 | Gruppo Lepetit S.P.A. | Antiinflammatory 2-imino-indolines and their pharmaceutical compositions |
-
0
- NL NL236636D patent/NL236636A/xx unknown
-
1959
- 1959-03-02 GB GB710559A patent/GB913931A/en not_active Expired
- 1959-03-03 DE DER25068A patent/DE1175238B/de active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3984563A (en) * | 1973-09-10 | 1976-10-05 | Gruppo Lepetit S.P.A. | Antiinflammatory 2-imino-indolines and their pharmaceutical compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| NL236636A (enrdf_load_stackoverflow) | |
| DE1175238B (de) | 1964-08-06 |
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