GB1527411A - Manufacture of 1,2-benzisothiazoles - Google Patents
Manufacture of 1,2-benzisothiazolesInfo
- Publication number
- GB1527411A GB1527411A GB348976A GB348976A GB1527411A GB 1527411 A GB1527411 A GB 1527411A GB 348976 A GB348976 A GB 348976A GB 348976 A GB348976 A GB 348976A GB 1527411 A GB1527411 A GB 1527411A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fused
- cycloaliphatic
- cyclohexyl
- jan
- 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
- CSNIZNHTOVFARY-UHFFFAOYSA-N 1,2-benzothiazole Chemical class C1=CC=C2C=NSC2=C1 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 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
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- -1 ethoxy, ethoxyphenyl Chemical group 0.000 abstract 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 125000005394 methallyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 abstract 1
- 125000003944 tolyl group Chemical group 0.000 abstract 1
- 125000005023 xylyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752503699 DE2503699C2 (de) | 1975-01-30 | 1975-01-30 | Verfahren zur Herstellung von 1,2- Benzisothiazolen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1527411A true GB1527411A (en) | 1978-10-04 |
Family
ID=5937625
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB348976A Expired GB1527411A (en) | 1975-01-30 | 1976-01-29 | Manufacture of 1,2-benzisothiazoles |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS51100070A (enrdf_load_stackoverflow) |
| AT (1) | AT346842B (enrdf_load_stackoverflow) |
| CH (1) | CH596196A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2503699C2 (enrdf_load_stackoverflow) |
| FR (1) | FR2299329A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1527411A (enrdf_load_stackoverflow) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2359834A1 (fr) * | 1976-07-26 | 1978-02-24 | Basf Ag | Nouveau napht(2,1-d)isothiazole et nematocides contenant ce compose |
| DE2734866A1 (de) | 1977-08-03 | 1979-02-22 | Basf Ag | Neue 1,2-benzisothiazole und verfahren zu ihrer herstellung |
| DE3018108A1 (de) | 1980-05-12 | 1981-11-19 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von 1,2-benzisothhiazolen |
| US5169951A (en) * | 1990-04-23 | 1992-12-08 | Ciba-Geigy Corporation | Process for preparing nematicidal compositions |
| DE59205384D1 (de) * | 1991-07-17 | 1996-03-28 | Ciba Geigy Ag | Nematizide Mittel |
| US5633384A (en) * | 1994-07-05 | 1997-05-27 | Sumitomo Seika Chemicals Co., Ltd. | Method for producing 1,2-benzisothiazol-3-ones |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1670196C3 (de) * | 1967-03-18 | 1975-09-18 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von 1,2-Benzisothiazolen |
-
1975
- 1975-01-30 DE DE19752503699 patent/DE2503699C2/de not_active Expired
-
1976
- 1976-01-27 CH CH102576A patent/CH596196A5/xx not_active IP Right Cessation
- 1976-01-29 AT AT63776A patent/AT346842B/de not_active IP Right Cessation
- 1976-01-29 GB GB348976A patent/GB1527411A/en not_active Expired
- 1976-01-29 FR FR7602368A patent/FR2299329A1/fr active Granted
- 1976-01-30 JP JP855776A patent/JPS51100070A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE2503699A1 (de) | 1976-08-05 |
| CH596196A5 (enrdf_load_stackoverflow) | 1978-03-15 |
| FR2299329A1 (fr) | 1976-08-27 |
| JPS51100070A (ja) | 1976-09-03 |
| ATA63776A (de) | 1978-04-15 |
| AT346842B (de) | 1978-11-27 |
| FR2299329B1 (enrdf_load_stackoverflow) | 1980-04-11 |
| DE2503699C2 (de) | 1983-04-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |