GB1340531A - Preparation of substituted chromenols - Google Patents
Preparation of substituted chromenolsInfo
- Publication number
- GB1340531A GB1340531A GB1340531DA GB1340531A GB 1340531 A GB1340531 A GB 1340531A GB 1340531D A GB1340531D A GB 1340531DA GB 1340531 A GB1340531 A GB 1340531A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chromenols
- substituted
- group
- chromenol
- hexyl
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
1340531 Heterocyclic-substituted chromenols BEECHAM GROUP Ltd 12 Jan 1972 [28 Jan 1971] 3354/71 Heading C2C A chromenol of Formula (I) or a salt thereof wherein R 1 is a C 1-20 hydrocarbon group, R 2 is a 6-membered heterocyclic group, with a nitrogen atom in the 4-position, R 3 a C 1-6 alkyl group, is obtained by reacting coumarin of Formula (II) with an alkali lithium compound R 3 Li and, if any intermediate triol (IV) is formed converting it, with or without isolation, by reaction with an acid to the chromenol (I), and if desired, forming a salt. Intermediate (II), in which R 2 is 4-pyridyl, Y is OH, and R 1 is n-butyl, n-hexyl, 2-hexyl or 2-heptyl, are obtained by reacting a mixture of ethyl iso-nicotinoylacetate and 5-(R 1 )-3,5-dihydroxy benzene with conc. sulphuric acid and/or phosphoryl chloride.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB335471 | 1971-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1340531A true GB1340531A (en) | 1973-12-12 |
Family
ID=9756735
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1340531D Expired GB1340531A (en) | 1971-01-28 | 1971-01-28 | Preparation of substituted chromenols |
Country Status (4)
Country | Link |
---|---|
CA (1) | CA981682A (en) |
CH (1) | CH577501A5 (en) |
ES (1) | ES399221A1 (en) |
GB (1) | GB1340531A (en) |
-
1971
- 1971-01-28 GB GB1340531D patent/GB1340531A/en not_active Expired
- 1971-12-30 CA CA131,429A patent/CA981682A/en not_active Expired
-
1972
- 1972-01-20 CH CH85872A patent/CH577501A5/xx not_active IP Right Cessation
- 1972-01-26 ES ES399221A patent/ES399221A1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
ES399221A1 (en) | 1974-11-16 |
CH577501A5 (en) | 1976-07-15 |
CA981682A (en) | 1976-01-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |