GB1034190A - Acylacetylamino compounds containing sulphuric acid ester groups and process for their manufacture - Google Patents
Acylacetylamino compounds containing sulphuric acid ester groups and process for their manufactureInfo
- Publication number
- GB1034190A GB1034190A GB33127/63A GB3312763A GB1034190A GB 1034190 A GB1034190 A GB 1034190A GB 33127/63 A GB33127/63 A GB 33127/63A GB 3312763 A GB3312763 A GB 3312763A GB 1034190 A GB1034190 A GB 1034190A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- prepared
- stearoylamino
- benzene
- acid
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 2
- 239000001117 sulphuric acid Substances 0.000 title abstract 2
- 235000011149 sulphuric acid Nutrition 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 3
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 3
- IKIPYYDVXNTYCJ-UHFFFAOYSA-N 1-(2,6-diamino-4-methoxyphenyl)octadecan-1-one Chemical compound NC1=C(C(=CC(=C1)OC)N)C(CCCCCCCCCCCCCCCCC)=O IKIPYYDVXNTYCJ-UHFFFAOYSA-N 0.000 abstract 2
- GKKZMYDNDDMXSE-UHFFFAOYSA-N Ethyl 3-oxo-3-phenylpropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=CC=C1 GKKZMYDNDDMXSE-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- RJOZGRQUCAXRNV-UHFFFAOYSA-N n-(4-ethoxyphenyl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC1=CC=C(OCC)C=C1 RJOZGRQUCAXRNV-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 2
- TUXQHZVZTVXXET-UHFFFAOYSA-N 1-(2,6-diamino-4-ethoxyphenyl)octadecan-1-one Chemical compound NC1=C(C(=CC(=C1)OCC)N)C(CCCCCCCCCCCCCCCCC)=O TUXQHZVZTVXXET-UHFFFAOYSA-N 0.000 abstract 1
- VHEXJWPABNGWCP-UHFFFAOYSA-N 1-(2,6-diamino-4-methoxyphenyl)dodecan-1-one Chemical compound NC1=C(C(=CC(=C1)OC)N)C(CCCCCCCCCCC)=O VHEXJWPABNGWCP-UHFFFAOYSA-N 0.000 abstract 1
- ALMQQYWSZUTWOR-UHFFFAOYSA-N 1-(4,5-diamino-2-methoxyphenyl)octadecan-1-one Chemical compound NC1=C(C=C(C(=C1)OC)C(CCCCCCCCCCCCCCCCC)=O)N ALMQQYWSZUTWOR-UHFFFAOYSA-N 0.000 abstract 1
- GVBHRNIWBGTNQA-UHFFFAOYSA-N 2-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC=C1N GVBHRNIWBGTNQA-UHFFFAOYSA-N 0.000 abstract 1
- IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 abstract 1
- QFMJFXFXQAFGBO-UHFFFAOYSA-N 4-methoxy-2-nitroaniline Chemical compound COC1=CC=C(N)C([N+]([O-])=O)=C1 QFMJFXFXQAFGBO-UHFFFAOYSA-N 0.000 abstract 1
- XWFSXIGWKPSRJG-UHFFFAOYSA-N N-(2-amino-4-ethoxyphenyl)octadecanamide Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC1=C(C=C(C=C1)OCC)N XWFSXIGWKPSRJG-UHFFFAOYSA-N 0.000 abstract 1
- WPPLXJGZRNJNGQ-UHFFFAOYSA-N N-(2-amino-4-methoxyphenyl)dodecanamide Chemical compound NC1=C(C=CC(=C1)OC)NC(CCCCCCCCCCC)=O WPPLXJGZRNJNGQ-UHFFFAOYSA-N 0.000 abstract 1
- KGZZBWVRDZAZFO-UHFFFAOYSA-N N-(2-amino-4-methoxyphenyl)octadecanamide Chemical compound NC1=C(C=CC(=C1)OC)NC(CCCCCCCCCCCCCCCCC)=O KGZZBWVRDZAZFO-UHFFFAOYSA-N 0.000 abstract 1
- VCJUANIJGKQNEP-UHFFFAOYSA-N N-(2-methoxy-4-nitrophenyl)octadecanamide Chemical compound [N+](=O)([O-])C=1C=CC(=C(C1)OC)NC(CCCCCCCCCCCCCCCCC)=O VCJUANIJGKQNEP-UHFFFAOYSA-N 0.000 abstract 1
- XMIUEPBOYRZDOO-UHFFFAOYSA-N N-(4-amino-2-methoxyphenyl)octadecanamide Chemical compound NC=1C=CC(=C(C1)OC)NC(CCCCCCCCCCCCCCCCC)=O XMIUEPBOYRZDOO-UHFFFAOYSA-N 0.000 abstract 1
- YKAHIFVDZJFZJT-UHFFFAOYSA-N N-(4-ethoxy-2-nitrophenyl)octadecanamide Chemical compound [N+](=O)([O-])C1=C(C=CC(=C1)OCC)NC(CCCCCCCCCCCCCCCCC)=O YKAHIFVDZJFZJT-UHFFFAOYSA-N 0.000 abstract 1
- HMSPSXWEHVIEMR-UHFFFAOYSA-N N-[2-[2-(octadecanoylamino)phenoxy]ethyl]benzamide Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC1=C(C=CC=C1)OCCNC(C1=CC=CC=C1)=O HMSPSXWEHVIEMR-UHFFFAOYSA-N 0.000 abstract 1
- MSHGOSCGWSSIGL-UHFFFAOYSA-N N-[6-methoxy-3-methyl-2-(octadecanoylamino)phenyl]benzamide Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC=1C(=C(C=CC1C)OC)NC(C1=CC=CC=C1)=O MSHGOSCGWSSIGL-UHFFFAOYSA-N 0.000 abstract 1
- PGQJNLHYYCNLNZ-UHFFFAOYSA-N N-[[2-(dodecanoylamino)phenoxy]methyl]benzamide Chemical compound C(CCCCCCCCCCC)(=O)NC1=C(C=CC=C1)OCNC(C1=CC=CC=C1)=O PGQJNLHYYCNLNZ-UHFFFAOYSA-N 0.000 abstract 1
- OUNPILGRHPCWPQ-UHFFFAOYSA-N N-[[2-(octadecanoylamino)phenoxy]methyl]benzamide Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC1=C(C=CC=C1)OCNC(C1=CC=CC=C1)=O OUNPILGRHPCWPQ-UHFFFAOYSA-N 0.000 abstract 1
- HPEZTTUIPKKLOE-UHFFFAOYSA-N N-[[2-(octadecanoylamino)phenoxy]methyl]cyclohexanecarboxamide Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC1=C(C=CC=C1)OCNC(C1CCCCC1)=O HPEZTTUIPKKLOE-UHFFFAOYSA-N 0.000 abstract 1
- 235000021355 Stearic acid Nutrition 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- NQGIJDNPUZEBRU-UHFFFAOYSA-N dodecanoyl chloride Chemical compound CCCCCCCCCCCC(Cl)=O NQGIJDNPUZEBRU-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- KRAHENMBSVAAHD-UHFFFAOYSA-N ethyl 3-(4-methoxyphenyl)-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=C(OC)C=C1 KRAHENMBSVAAHD-UHFFFAOYSA-N 0.000 abstract 1
- GEQMJBPKCOZHMV-UHFFFAOYSA-N ethyl 3-(4-methylphenyl)-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=C(C)C=C1 GEQMJBPKCOZHMV-UHFFFAOYSA-N 0.000 abstract 1
- ASYASKBLHYSMEG-UHFFFAOYSA-N ethyl 3-cyclohexyl-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)C1CCCCC1 ASYASKBLHYSMEG-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- WRGLZAJBHUOPFO-UHFFFAOYSA-N methyl 3-oxo-3-phenylpropanoate Chemical compound COC(=O)CC(=O)C1=CC=CC=C1 WRGLZAJBHUOPFO-UHFFFAOYSA-N 0.000 abstract 1
- XQLVSULNBOAZLP-UHFFFAOYSA-N n-(4-methoxy-2-nitrophenyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC1=CC=C(OC)C=C1[N+]([O-])=O XQLVSULNBOAZLP-UHFFFAOYSA-N 0.000 abstract 1
- 230000000802 nitrating effect Effects 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 1
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical group 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000008117 stearic acid Substances 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/36—Couplers containing compounds with active methylene groups
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/36—Desensitisers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1040062A CH455514A (de) | 1962-08-31 | 1962-08-31 | Verwendung von Schwefelsäureestergruppen enthaltenden Acetylaminoverbindungen als Farbkuppler |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1034190A true GB1034190A (en) | 1966-06-29 |
Family
ID=4362816
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB33127/63A Expired GB1034190A (en) | 1962-08-31 | 1963-08-21 | Acylacetylamino compounds containing sulphuric acid ester groups and process for their manufacture |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3472145A (enEXAMPLES) |
| AT (1) | AT243083B (enEXAMPLES) |
| BE (1) | BE636700A (enEXAMPLES) |
| CH (1) | CH455514A (enEXAMPLES) |
| DE (1) | DE1447600A1 (enEXAMPLES) |
| ES (1) | ES291252A1 (enEXAMPLES) |
| GB (1) | GB1034190A (enEXAMPLES) |
| NL (1) | NL297348A (enEXAMPLES) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2407210A (en) * | 1944-04-14 | 1946-09-03 | Eastman Kodak Co | Color couplers |
| BE497011A (enEXAMPLES) * | 1949-07-16 | |||
| BE543742A (enEXAMPLES) * | 1954-12-20 | |||
| GB784422A (en) * | 1955-01-29 | 1957-10-09 | Ilford Ltd | Improvements in or relating to colour photography |
-
0
- BE BE636700D patent/BE636700A/xx unknown
- NL NL297348D patent/NL297348A/xx unknown
-
1962
- 1962-08-31 CH CH1040062A patent/CH455514A/de unknown
-
1963
- 1963-08-21 GB GB33127/63A patent/GB1034190A/en not_active Expired
- 1963-08-30 DE DE19631447600 patent/DE1447600A1/de active Pending
- 1963-08-30 AT AT700163A patent/AT243083B/de active
- 1963-08-30 ES ES291252A patent/ES291252A1/es not_active Expired
-
1967
- 1967-12-21 US US692311A patent/US3472145A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE1447600A1 (de) | 1969-01-23 |
| CH455514A (de) | 1968-07-15 |
| ES291252A1 (es) | 1964-04-01 |
| NL297348A (enEXAMPLES) | |
| US3472145A (en) | 1969-10-14 |
| BE636700A (enEXAMPLES) | |
| AT243083B (de) | 1965-10-25 |
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