GB1264737A - - Google Patents
Info
- Publication number
- GB1264737A GB1264737A GB1264737DA GB1264737A GB 1264737 A GB1264737 A GB 1264737A GB 1264737D A GB1264737D A GB 1264737DA GB 1264737 A GB1264737 A GB 1264737A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkoxy
- alkyl
- amino
- methylthiophenylthio
- methylthio
- 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
- -1 polyhydroxyalkoxy Chemical group 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 abstract 2
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 abstract 1
- VYGXLDXWNLTGIL-UHFFFAOYSA-N 1-methylsulfanyl-4-(trifluoromethyl)benzene Chemical compound CSC1=CC=C(C(F)(F)F)C=C1 VYGXLDXWNLTGIL-UHFFFAOYSA-N 0.000 abstract 1
- AHJDVRKSMLDZEY-UHFFFAOYSA-N 4-(4-methylsulfanylphenyl)sulfanylphenol Chemical compound CSC1=CC=C(C=C1)SC1=CC=C(C=C1)O AHJDVRKSMLDZEY-UHFFFAOYSA-N 0.000 abstract 1
- WCMLRSZJUIKVCW-UHFFFAOYSA-N 4-(trifluoromethyl)benzenethiol Chemical compound FC(F)(F)C1=CC=C(S)C=C1 WCMLRSZJUIKVCW-UHFFFAOYSA-N 0.000 abstract 1
- PJHWTWHVCOZCPU-UHFFFAOYSA-N 4-methylbenzenecarbothioic s-acid Chemical compound CC1=CC=C(C(O)=S)C=C1 PJHWTWHVCOZCPU-UHFFFAOYSA-N 0.000 abstract 1
- BVVRIOODSNPWHJ-UHFFFAOYSA-N CSC1=CC=C(C=C1)SC1=CC=C(C=C1)OC Chemical compound CSC1=CC=C(C=C1)SC1=CC=C(C=C1)OC BVVRIOODSNPWHJ-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-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
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 1
- 125000000278 alkyl amino alkyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001413 amino acids Chemical class 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 230000000202 analgesic effect Effects 0.000 abstract 1
- 230000001567 anti-fibrinolytic effect Effects 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000001754 anti-pyretic effect Effects 0.000 abstract 1
- 229940082620 antifibrinolytics Drugs 0.000 abstract 1
- 239000002221 antipyretic Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- BGXZJSLTGNPDDH-UHFFFAOYSA-N benzenethiol;sodium Chemical compound [Na].SC1=CC=CC=C1 BGXZJSLTGNPDDH-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 230000001335 demethylating effect Effects 0.000 abstract 1
- 230000017858 demethylation Effects 0.000 abstract 1
- 238000010520 demethylation reaction Methods 0.000 abstract 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 1
- 125000004984 dialkylaminoalkoxy group Chemical group 0.000 abstract 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002934 diuretic Substances 0.000 abstract 1
- 230000001882 diuretic effect Effects 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000005191 hydroxyalkylamino group Chemical group 0.000 abstract 1
- 230000002218 hypoglycaemic effect Effects 0.000 abstract 1
- 125000005358 mercaptoalkyl group Chemical group 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 229940058287 salicylic acid derivative anticestodals Drugs 0.000 abstract 1
- 150000003872 salicylic acid derivatives Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000010561 standard procedure Methods 0.000 abstract 1
- QHMQWEPBXSHHLH-UHFFFAOYSA-N sulfur tetrafluoride Chemical compound FS(F)(F)F QHMQWEPBXSHHLH-UHFFFAOYSA-N 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83661169A | 1969-06-25 | 1969-06-25 | |
| US3031970A | 1970-04-20 | 1970-04-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1264737A true GB1264737A (enrdf_load_stackoverflow) | 1972-02-23 |
Family
ID=26705903
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1264737D Expired GB1264737A (enrdf_load_stackoverflow) | 1969-06-25 | 1970-06-18 |
Country Status (5)
| Country | Link |
|---|---|
| CA (1) | CA960227A (enrdf_load_stackoverflow) |
| DE (1) | DE2031229A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2053014B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1264737A (enrdf_load_stackoverflow) |
| NL (1) | NL7008629A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2259239A1 (de) * | 1972-07-19 | 1974-02-14 | Renfag Sa | Verfahren zur herstellung von 2alkoxy-5-alkylsulfonyl-benzoesaeure |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9214120D0 (en) * | 1991-07-25 | 1992-08-12 | Ici Plc | Therapeutic amides |
| GB9305295D0 (en) * | 1993-03-15 | 1993-05-05 | Zeneca Ltd | Therapeutic compounds |
| GB9310095D0 (en) * | 1993-05-17 | 1993-06-30 | Zeneca Ltd | Therapeutic compounds |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1841636A (en) * | 1925-07-31 | 1932-01-19 | British Dyestuffs Corp Ltd | Amino and nitro derivatives of ortho-hydroxy-carboxy-diphenyl sulphides, and process of preparing same |
| US2445939A (en) * | 1941-10-31 | 1948-07-27 | American Cyanamid Co | Metal salts of acyl phenol monosulfides |
| US2761873A (en) * | 1953-11-04 | 1956-09-04 | Du Pont | Preparation of 4-substituted mercaptophenyl aldehydes and ketones |
-
1970
- 1970-06-12 NL NL7008629A patent/NL7008629A/xx unknown
- 1970-06-15 CA CA085,561A patent/CA960227A/en not_active Expired
- 1970-06-18 GB GB1264737D patent/GB1264737A/en not_active Expired
- 1970-06-24 DE DE19702031229 patent/DE2031229A1/de active Pending
- 1970-06-24 FR FR7023327A patent/FR2053014B1/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2259239A1 (de) * | 1972-07-19 | 1974-02-14 | Renfag Sa | Verfahren zur herstellung von 2alkoxy-5-alkylsulfonyl-benzoesaeure |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2053014A1 (enrdf_load_stackoverflow) | 1971-04-16 |
| FR2053014B1 (enrdf_load_stackoverflow) | 1973-08-10 |
| NL7008629A (enrdf_load_stackoverflow) | 1970-12-29 |
| CA960227A (en) | 1974-12-31 |
| DE2031229A1 (de) | 1971-01-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1419608A (en) | Aroyl-substituted naphthaleneacetic acids and their derivatives | |
| GB1496580A (en) | 3-cyanopyridine derivatives | |
| GB1467927A (en) | Derivatives of tyrosine having a pharmaceutical activity on smooth muscles | |
| GB1269551A (en) | New tricyclic derivatives and process for their manufacture | |
| GB1268465A (en) | Substituted salicylic acid compounds | |
| GB1264737A (enrdf_load_stackoverflow) | ||
| GB1187259A (en) | New Aminoalkyl Esters of 2-Anilino-Nicotinic Acids and process for their manufacture | |
| GB1397645A (en) | Aza-benzimidazoles | |
| GB1271466A (en) | Thiocarbamic acid derivatives | |
| GB1462036A (en) | Aminoindane derivatives | |
| GB1475314A (en) | Phenyl-propylamine derivatives | |
| GB1315830A (en) | Halophenyl-2-hydroxyphenylacetic acids and their derivatives | |
| GB1157100A (en) | Pharmaceutical Compositions | |
| GB1432660A (en) | Piperazine derivatives processes for their preparation and and pharamacueitcal compositions containing them | |
| GB1173222A (en) | Substituted 6,7-Benzomorphans and their Preparation | |
| GB1508276A (en) | Oxamic and dioxamic acid derivatives | |
| GB1222179A (en) | A process for the preparation of sulfonyl urea derivatives | |
| GB1268469A (en) | Halomethylquinolylamino-benzamides | |
| GB1265924A (enrdf_load_stackoverflow) | ||
| GB1415682A (en) | Amides and thioamides | |
| GB1501592A (en) | Pharmaceutical compositions | |
| GB1533048A (en) | Antiperspirant compositions and methods of producing them | |
| GB1219387A (en) | Bicyclo[2.2.2]oct-2-ene-amino acid compounds | |
| GB1166758A (en) | Phenoxyacetic Acids | |
| IE34139L (en) | 4-phenyl-butyric acid derivatives |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |