FI79699B - Foerfarande foer framstaellning av indol och en mellanprodukt. - Google Patents
Foerfarande foer framstaellning av indol och en mellanprodukt. Download PDFInfo
- Publication number
- FI79699B FI79699B FI844788A FI844788A FI79699B FI 79699 B FI79699 B FI 79699B FI 844788 A FI844788 A FI 844788A FI 844788 A FI844788 A FI 844788A FI 79699 B FI79699 B FI 79699B
- Authority
- FI
- Finland
- Prior art keywords
- group
- general formula
- compound
- hydrogen atom
- alkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
- C07D209/16—Tryptamines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Claims (2)
1. Förfarande för framställning av indol med den allmänna formeln (I) R]R2NS02CHR3 AlkNR4R5 XX/ H där Rl är en väteatom eller Ci_g alkyl eller ¢3.5 alkenylgrupp; R2 är en väteatom eller Ci_3 alkyl-, fenyl- eller fen(Ci_4)-alkylgrupp; R3 är en väteatom, R4 och R5, vilka kan vara likadana eller olika, är var och en väteatom eller Ci_3 alkyl- eller propenylgrupp eller R4 och R5 tillsammans bildar en bensylidengrupp; och Alk är en alkylenkedja med 2 eller 3 kolatomer, eller deras fysiologiskt godtagbara sait eller soivat, kännetecknat därav, att (A) en indol med den allmänna formeln (II) XS02CHR3 AlkNR4R5 XXX H där X är en grupp ORg, där Rg är en hydrokarbylgrupp och R3, R4, R5 och Alk avser samma som i den allmänna formeln (I), bringas att reagera med en förening med den allmänna formeln (III) i9 79699 RK NH (III) *2^ (där R^ och R2 avser samma som i den allmänna formeln (I)); och vid behov och/eller om sa önskas, underkastas den erhallna föreningen en eller flera av följande reaktioner, där (B) (i) en förening med den allmänna formeln (I) eller dess salt eller skyddade derivat omvandlas till en annan förening med den allmänna formeln (I); (ii) avlägsnas en eventuell skyddsgrupp eller -grupper; (iii) omvandlas en förening med den allmänna formeln (I) eller dess salt till sitt fysiologiskt lämpliga salt eller soivat.
2. En förening med den allmänna formeln (II) XSO2CHR3 AlkNR4R5 —Z (II) XXj H där R3 är en väteatom; R4 och R5, vilka kan vara likadana eller olika, är vardera en väteatom eller Ci_3 alkylgrupp; Alk är en alkylenkedja med 2 eller 3 kolatomer, och X är fenoxi, och deras salter.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB838332434A GB8332434D0 (en) | 1983-12-06 | 1983-12-06 | Production of chemical compounds |
GB8332434 | 1983-12-06 |
Publications (4)
Publication Number | Publication Date |
---|---|
FI844788A0 FI844788A0 (fi) | 1984-12-05 |
FI844788L FI844788L (fi) | 1985-06-07 |
FI79699B true FI79699B (fi) | 1989-10-31 |
FI79699C FI79699C (sv) | 1990-02-12 |
Family
ID=10552844
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI844788A FI79699C (sv) | 1983-12-06 | 1984-12-05 | Förfarande för framställning av indol och en mellanprodukt |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0145459A3 (sv) |
JP (1) | JPS60139669A (sv) |
KR (1) | KR920000895B1 (sv) |
CA (1) | CA1230602A (sv) |
ES (1) | ES538335A0 (sv) |
FI (1) | FI79699C (sv) |
GB (1) | GB8332434D0 (sv) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8419575D0 (en) * | 1984-08-01 | 1984-09-05 | Glaxo Group Ltd | Chemical compounds |
DE3678805D1 (de) * | 1985-11-08 | 1991-05-23 | Glaxo Group Ltd | Indolderivate. |
GB8600397D0 (en) * | 1986-01-08 | 1986-02-12 | Glaxo Group Ltd | Chemical compounds |
GB8601959D0 (en) * | 1986-01-28 | 1986-03-05 | Glaxo Group Ltd | Indole derivatives |
US5270333A (en) * | 1986-01-28 | 1993-12-14 | Glaxo Group Limited | Indole derivatives |
US5225431A (en) * | 1987-10-23 | 1993-07-06 | Burroughs Wellcome Co. | Therapeutic substituted indole compounds and compositions thereof |
ES2033578B1 (es) * | 1991-06-06 | 1995-01-16 | Quimica Sint S A Con El 50 | Procedimiento para la obtencion de 3-(2-(dimetilamino)etil)-n-metil-1h-indol-5-metanosulfonamida. |
ES2055651B1 (es) * | 1992-07-20 | 1995-03-01 | Vita Invest Sa | Procedimiento para la obtencion de nuevas amidinas derivadas de 3-aminoetilindoles. |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3472870A (en) * | 1966-08-29 | 1969-10-14 | Mead Johnson & Co | Sulfonamidotryptamines |
ZW19381A1 (en) * | 1980-08-12 | 1983-03-09 | Glaxo Group Ltd | Heterocyclic compounds |
IT1170387B (it) * | 1982-06-07 | 1987-06-03 | Glaxo Group Ltd | Composti eterociclici, procedimento per prepararli e composizioni farmaceutiche che li contengono |
-
1983
- 1983-12-06 GB GB838332434A patent/GB8332434D0/en active Pending
-
1984
- 1984-12-05 FI FI844788A patent/FI79699C/sv active IP Right Grant
- 1984-12-06 EP EP84308492A patent/EP0145459A3/en not_active Withdrawn
- 1984-12-06 JP JP59258410A patent/JPS60139669A/ja active Pending
- 1984-12-06 ES ES538335A patent/ES538335A0/es active Granted
- 1984-12-06 CA CA000469527A patent/CA1230602A/en not_active Expired
- 1984-12-06 KR KR1019840007710A patent/KR920000895B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
KR920000895B1 (ko) | 1992-01-30 |
EP0145459A3 (en) | 1985-07-10 |
KR850004460A (ko) | 1985-07-15 |
ES8603822A1 (es) | 1986-01-01 |
FI844788A0 (fi) | 1984-12-05 |
CA1230602A (en) | 1987-12-22 |
GB8332434D0 (en) | 1984-01-11 |
ES538335A0 (es) | 1986-01-01 |
FI844788L (fi) | 1985-06-07 |
FI79699C (sv) | 1990-02-12 |
JPS60139669A (ja) | 1985-07-24 |
EP0145459A2 (en) | 1985-06-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Patent granted |
Owner name: GLAXO GROUP LIMITED |