GB1028913A - Basically substituted diphenyl-methyl ethers, processes for their manufacture and their use - Google Patents
Basically substituted diphenyl-methyl ethers, processes for their manufacture and their useInfo
- Publication number
- GB1028913A GB1028913A GB5541/63A GB554163A GB1028913A GB 1028913 A GB1028913 A GB 1028913A GB 5541/63 A GB5541/63 A GB 5541/63A GB 554163 A GB554163 A GB 554163A GB 1028913 A GB1028913 A GB 1028913A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compound
- phenyl
- formula
- hydrogen atom
- condensing
- 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
- PVQATPQSBYNMGE-UHFFFAOYSA-N [benzhydryloxy(phenyl)methyl]benzene Chemical class C=1C=CC=CC=1C(C=1C=CC=CC=1)OC(C=1C=CC=CC=1)C1=CC=CC=C1 PVQATPQSBYNMGE-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 5
- -1 phenyl acetone compound Chemical class 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- RMMRRRLPDBJBQL-UHFFFAOYSA-N 1-(3-methoxyphenyl)propan-2-one Chemical compound COC1=CC=CC(CC(C)=O)=C1 RMMRRRLPDBJBQL-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- BNSBFWVSQWAIRE-UHFFFAOYSA-N N-(2-chloroethyl)-1-(3,4-dimethoxyphenyl)-N-methylpropan-2-amine Chemical compound COC=1C=C(C=CC1OC)CC(C)N(C)CCCl BNSBFWVSQWAIRE-UHFFFAOYSA-N 0.000 abstract 1
- VWFZGPKSVWBLTP-UHFFFAOYSA-N N-(2-chloroethyl)-1-(3,5-dimethoxyphenyl)-N-methylpropan-2-amine Chemical compound COC1=CC(OC)=CC(CC(C)N(C)CCCl)=C1 VWFZGPKSVWBLTP-UHFFFAOYSA-N 0.000 abstract 1
- FAQZKFBRUIJLMN-UHFFFAOYSA-N N-(2-chloroethyl)-1-(3-methoxyphenyl)-N-methylpropan-2-amine Chemical compound COC1=CC=CC(CC(C)N(C)CCCl)=C1 FAQZKFBRUIJLMN-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000017531 blood circulation Effects 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 229950000188 halopropane Drugs 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 230000001035 methylating effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000001766 physiological effect Effects 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Landscapes
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0035984 | 1962-02-09 | ||
| DEF0037514 | 1962-08-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1028913A true GB1028913A (en) | 1966-05-11 |
Family
ID=25975230
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5541/63A Expired GB1028913A (en) | 1962-02-09 | 1963-02-11 | Basically substituted diphenyl-methyl ethers, processes for their manufacture and their use |
Country Status (11)
| Country | Link |
|---|---|
| AT (6) | AT242686B (enrdf_load_stackoverflow) |
| BE (1) | BE628262A (enrdf_load_stackoverflow) |
| BR (1) | BR6346803D0 (enrdf_load_stackoverflow) |
| CH (6) | CH460047A (enrdf_load_stackoverflow) |
| DE (1) | DE1245981B (enrdf_load_stackoverflow) |
| DK (4) | DK104989C (enrdf_load_stackoverflow) |
| FI (1) | FI40722B (enrdf_load_stackoverflow) |
| FR (1) | FR2880M (enrdf_load_stackoverflow) |
| GB (1) | GB1028913A (enrdf_load_stackoverflow) |
| NL (1) | NL288538A (enrdf_load_stackoverflow) |
| OA (1) | OA02646A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5171752A (en) * | 1990-07-19 | 1992-12-15 | Akzo N.V. | Benzhydryl derivatives having calmodulin inhibitor properties |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8824262D0 (en) * | 1988-10-17 | 1988-11-23 | Pfizer Ltd | Therapeutic agents |
-
0
- DE DENDAT1245981D patent/DE1245981B/de active Pending
- NL NL288538D patent/NL288538A/xx unknown
- BE BE628262D patent/BE628262A/xx unknown
-
1963
- 1963-02-07 AT AT281864A patent/AT242686B/de active
- 1963-02-07 AT AT281664A patent/AT242684B/de active
- 1963-02-07 AT AT95663A patent/AT242119B/de active
- 1963-02-07 CH CH121267A patent/CH460047A/de unknown
- 1963-02-07 CH CH121467A patent/CH460049A/de unknown
- 1963-02-07 CH CH152463A patent/CH443352A/de unknown
- 1963-02-07 AT AT281964A patent/AT242687B/de active
- 1963-02-07 CH CH121367A patent/CH460048A/de unknown
- 1963-02-07 AT AT281564A patent/AT242683B/de active
- 1963-02-07 AT AT281764A patent/AT242685B/de active
- 1963-02-07 CH CH121167A patent/CH460046A/de unknown
- 1963-02-07 CH CH121067A patent/CH460811A/de unknown
- 1963-02-08 FI FI24163A patent/FI40722B/fi active
- 1963-02-08 DK DK423664A patent/DK104989C/da active
- 1963-02-08 BR BR14680363A patent/BR6346803D0/pt unknown
- 1963-02-08 DK DK423464A patent/DK106283C/da active
- 1963-02-08 DK DK423764A patent/DK104890C/da active
- 1963-02-08 DK DK61263A patent/DK104943C/da active
- 1963-02-11 GB GB5541/63A patent/GB1028913A/en not_active Expired
- 1963-05-08 FR FR934139A patent/FR2880M/fr active Active
-
1964
- 1964-12-31 OA OA51808A patent/OA02646A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5171752A (en) * | 1990-07-19 | 1992-12-15 | Akzo N.V. | Benzhydryl derivatives having calmodulin inhibitor properties |
Also Published As
| Publication number | Publication date |
|---|---|
| FI40722B (enrdf_load_stackoverflow) | 1969-01-31 |
| BE628262A (enrdf_load_stackoverflow) | |
| AT242686B (de) | 1965-09-27 |
| AT242687B (de) | 1965-09-27 |
| NL288538A (enrdf_load_stackoverflow) | |
| AT242684B (de) | 1965-09-27 |
| FR2880M (fr) | 1964-11-02 |
| CH460046A (de) | 1968-07-31 |
| CH460048A (de) | 1968-07-31 |
| CH460811A (de) | 1968-08-15 |
| DK104989C (da) | 1966-08-01 |
| AT242685B (de) | 1965-09-27 |
| OA02646A (fr) | 1970-12-15 |
| BR6346803D0 (pt) | 1973-06-14 |
| DE1245981B (de) | 1967-08-03 |
| DK104890C (da) | 1966-07-18 |
| CH443352A (de) | 1967-09-15 |
| CH460047A (de) | 1968-07-31 |
| DK106283C (da) | 1967-01-16 |
| AT242683B (de) | 1965-09-27 |
| CH460049A (de) | 1968-07-31 |
| AT242119B (de) | 1965-08-25 |
| DK104943C (da) | 1966-07-25 |
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