GB1018773A - ª‡-phenyl-ª‰-2-furyl-propionitrile derivatives - Google Patents
ª‡-phenyl-ª‰-2-furyl-propionitrile derivativesInfo
- Publication number
- GB1018773A GB1018773A GB35021/62A GB3502162A GB1018773A GB 1018773 A GB1018773 A GB 1018773A GB 35021/62 A GB35021/62 A GB 35021/62A GB 3502162 A GB3502162 A GB 3502162A GB 1018773 A GB1018773 A GB 1018773A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- furyl
- lower alkyl
- alkali metal
- formula
- 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
- 229910052783 alkali metal Inorganic materials 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- SUSQOBVLVYHIEX-UHFFFAOYSA-N phenylacetonitrile Chemical compound N#CCC1=CC=CC=C1 SUSQOBVLVYHIEX-UHFFFAOYSA-N 0.000 abstract 4
- 150000001340 alkali metals Chemical class 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- GANBJDIOIDQSGI-UHFFFAOYSA-N 2-(chloromethyl)furan Chemical compound ClCC1=CC=CO1 GANBJDIOIDQSGI-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- -1 alkali metal amide Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 230000003444 anaesthetic effect Effects 0.000 abstract 1
- 230000000954 anitussive effect Effects 0.000 abstract 1
- 229940124584 antitussives Drugs 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 239000003874 central nervous system depressant Substances 0.000 abstract 1
- 239000003610 charcoal Substances 0.000 abstract 1
- 239000000812 cholinergic antagonist Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 239000003589 local anesthetic agent Substances 0.000 abstract 1
- GFTXWCQFWLOXAT-UHFFFAOYSA-M magnesium;cyclohexane;bromide Chemical compound [Mg+2].[Br-].C1CC[CH-]CC1 GFTXWCQFWLOXAT-UHFFFAOYSA-M 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 150000003385 sodium Chemical class 0.000 abstract 1
- 230000002048 spasmolytic effect Effects 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB35021/62A GB1018773A (en) | 1962-09-13 | 1962-09-13 | ª‡-phenyl-ª‰-2-furyl-propionitrile derivatives |
| FR946501A FR1567852A (https=) | 1962-09-13 | 1963-09-04 | |
| FR980550A FR93951E (fr) | 1962-09-13 | 1964-07-03 | Procédé de préparation des dérivés de l'alpha-phényl beta furyl-2 propionitrile. |
| DE1964L0048541 DE1240089B (de) | 1962-09-13 | 1964-08-14 | Verfahren zur Herstellung von alpha-Phenyl-beta-furyl-(2)-propionitril |
| US402312A US3272827A (en) | 1962-09-13 | 1964-10-07 | Alpha-phenyl-beta-(2-furyl propionitrile compounds and a process of making same |
| FR41404A FR93952E (fr) | 1962-09-13 | 1965-12-08 | Procédé de préparation des dérivés de l'alpha-phényl beta (furyl-2) propionitrile. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB35021/62A GB1018773A (en) | 1962-09-13 | 1962-09-13 | ª‡-phenyl-ª‰-2-furyl-propionitrile derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1018773A true GB1018773A (en) | 1966-02-02 |
Family
ID=10372854
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB35021/62A Expired GB1018773A (en) | 1962-09-13 | 1962-09-13 | ª‡-phenyl-ª‰-2-furyl-propionitrile derivatives |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US3272827A (https=) |
| FR (1) | FR1567852A (https=) |
| GB (1) | GB1018773A (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2350323C2 (ru) * | 2002-10-11 | 2009-03-27 | Бакстер Интернэшнл Инк. | Способ кардиопротекции и нейропротекции внутривенным введением галогенсодержащего летучего анестезирующего средства |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4057549A (en) * | 1975-04-16 | 1977-11-08 | G. D. Searle & Co. | Triarylpropyl-azabicyclooctanes |
| US20030136859A1 (en) | 2002-01-18 | 2003-07-24 | 3M Innovative Properties Company | Method of applying two-component pavement markings and apparatus |
| WO2005047604A1 (en) | 2003-11-06 | 2005-05-26 | 3M Innovative Properties Company | Retroreflective elements comprising a bonded resin core and pavement markings |
| US7513941B2 (en) | 2005-11-14 | 2009-04-07 | 3M Innovative Properties Company | Pavement marking, reflective elements, and methods of making micospheres |
| US20080280034A1 (en) * | 2007-05-11 | 2008-11-13 | 3M Innovative Properties Company | Pavement marking and reflective elements having microspheres comprising lanthanum oxide and aluminum oxide with zirconia, titania, or mixtures thereof |
| WO2011022022A1 (en) | 2009-08-21 | 2011-02-24 | 3M Innovative Properties Company | Pavement markings, reflective elements, and methods of making microspheres |
| WO2023170516A1 (en) | 2022-03-09 | 2023-09-14 | 3M Innovative Properties Company | Microspheres comprising zirconia and alumina suitable for retroreflective articles |
| JP2025509209A (ja) | 2022-03-09 | 2025-04-11 | スリーエム イノベイティブ プロパティズ カンパニー | 再帰反射性物品に好適なアルミナ及びジルコニアを含むマイクロスフィア |
| WO2024003637A1 (en) | 2022-06-29 | 2024-01-04 | 3M Innovative Properties Company | Curable adhesive and articles for bonding pavement and concrete |
| WO2026003616A1 (en) | 2024-06-28 | 2026-01-02 | 3M Innovative Properties Company | Glass microspheres and articles thereof |
| WO2026003617A1 (en) | 2024-06-28 | 2026-01-02 | 3M Innovative Properties Company | Microspheres and articles thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE620631A (https=) * | ||||
| GB776705A (en) * | 1954-06-05 | 1957-06-12 | Henri Morren | New dialkylamino derivatives and process for the production thereof |
-
1962
- 1962-09-13 GB GB35021/62A patent/GB1018773A/en not_active Expired
-
1963
- 1963-09-04 FR FR946501A patent/FR1567852A/fr not_active Expired
-
1964
- 1964-10-07 US US402312A patent/US3272827A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2350323C2 (ru) * | 2002-10-11 | 2009-03-27 | Бакстер Интернэшнл Инк. | Способ кардиопротекции и нейропротекции внутривенным введением галогенсодержащего летучего анестезирующего средства |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1567852A (https=) | 1969-05-23 |
| US3272827A (en) | 1966-09-13 |
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