GB1415207A - Process for the manufacture of nuclear-sulphonated compounds - Google Patents
Process for the manufacture of nuclear-sulphonated compoundsInfo
- Publication number
- GB1415207A GB1415207A GB1196573A GB1196573A GB1415207A GB 1415207 A GB1415207 A GB 1415207A GB 1196573 A GB1196573 A GB 1196573A GB 1196573 A GB1196573 A GB 1196573A GB 1415207 A GB1415207 A GB 1415207A
- Authority
- GB
- United Kingdom
- Prior art keywords
- unsubstituted
- substituted
- group
- aromatic
- denotes
- 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 2
- 238000000034 method Methods 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- -1 heterocyclic amine Chemical class 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- 125000001931 aliphatic group Chemical group 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 abstract 2
- 239000000010 aprotic solvent Substances 0.000 abstract 2
- 150000005840 aryl radicals Chemical class 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 abstract 1
- GGYVTHJIUNGKFZ-UHFFFAOYSA-N 1-methylpiperidin-2-one Chemical compound CN1CCCCC1=O GGYVTHJIUNGKFZ-UHFFFAOYSA-N 0.000 abstract 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 abstract 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N Caprolactam Natural products O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 abstract 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 abstract 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000001491 aromatic compounds Chemical class 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 150000008378 aryl ethers Chemical class 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000001174 sulfone group Chemical group 0.000 abstract 1
- 150000003568 thioethers Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/22—Dyes with unsubstituted amino groups
- C09B1/24—Dyes with unsubstituted amino groups sulfonated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH393972A CH570975A5 (enExample) | 1972-03-16 | 1972-03-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1415207A true GB1415207A (en) | 1975-11-26 |
Family
ID=4266732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1196573A Expired GB1415207A (en) | 1972-03-16 | 1973-03-13 | Process for the manufacture of nuclear-sulphonated compounds |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS5929073B2 (enExample) |
| BE (1) | BE796812A (enExample) |
| CA (1) | CA1023733A (enExample) |
| CH (1) | CH570975A5 (enExample) |
| DE (1) | DE2312728A1 (enExample) |
| FR (1) | FR2175790B1 (enExample) |
| GB (1) | GB1415207A (enExample) |
| IT (1) | IT979836B (enExample) |
| NL (1) | NL7303648A (enExample) |
| SE (1) | SE416200B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS606323B2 (ja) * | 1978-12-26 | 1985-02-18 | 清 五月女 | 植物を保護する方法 |
| DE3114830A1 (de) * | 1981-04-11 | 1982-11-04 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von amino-arylsulfonsaeuren |
| FR2727410B1 (fr) * | 1994-11-25 | 1996-12-20 | Synthelabo | Chlorures de sulfonyles, leur preparation et leur utilisation comme intermediaires de synthese |
| CA2610903A1 (en) | 2005-06-16 | 2006-12-21 | Pfizer Inc. | N-(pyridin-2-yl)-sulfonamide derivatives |
| JP4885621B2 (ja) * | 2006-06-09 | 2012-02-29 | ユニクラフトナグラ株式会社 | リング状溝逐次転造方法及びリング状溝逐次転造装置 |
| JP6815603B2 (ja) * | 2016-11-22 | 2021-01-20 | スガイ化学工業株式会社 | ジナフトチオフェン誘導体及びその製造方法 |
-
1972
- 1972-03-16 CH CH393972A patent/CH570975A5/xx not_active IP Right Cessation
-
1973
- 1973-02-09 SE SE7301823A patent/SE416200B/xx unknown
- 1973-03-06 FR FR7308001A patent/FR2175790B1/fr not_active Expired
- 1973-03-06 CA CA165,335A patent/CA1023733A/en not_active Expired
- 1973-03-13 GB GB1196573A patent/GB1415207A/en not_active Expired
- 1973-03-14 DE DE19732312728 patent/DE2312728A1/de not_active Ceased
- 1973-03-14 IT IT4879173A patent/IT979836B/it active
- 1973-03-15 NL NL7303648A patent/NL7303648A/xx not_active Application Discontinuation
- 1973-03-15 BE BE128821A patent/BE796812A/xx not_active IP Right Cessation
- 1973-03-16 JP JP48030147A patent/JPS5929073B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2175790B1 (enExample) | 1976-05-21 |
| JPS5929073B2 (ja) | 1984-07-18 |
| FR2175790A1 (enExample) | 1973-10-26 |
| SE416200B (sv) | 1980-12-08 |
| BE796812A (fr) | 1973-09-17 |
| IT979836B (it) | 1974-09-30 |
| JPS491536A (enExample) | 1974-01-08 |
| NL7303648A (enExample) | 1973-09-18 |
| CA1023733A (en) | 1978-01-03 |
| DE2312728A1 (de) | 1973-09-20 |
| CH570975A5 (enExample) | 1975-12-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |