GB973142A - (4-acetyl-1-naphthoxy) propyl esters - Google Patents
(4-acetyl-1-naphthoxy) propyl estersInfo
- Publication number
- GB973142A GB973142A GB2450560A GB2450560A GB973142A GB 973142 A GB973142 A GB 973142A GB 2450560 A GB2450560 A GB 2450560A GB 2450560 A GB2450560 A GB 2450560A GB 973142 A GB973142 A GB 973142A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- carry
- substituent
- carboxyl
- tri
- 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
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/73—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
Abstract
The invention comprises esters of the general formula <FORM:0973142/C1/1> (wherein R represents either (a) the group -COR, in which R1 represents a C1-5 alkyl group which may carry a halogen or an o -carboxyl substituent, a phenyl group which may carry a carboxyl or sulphonic substituent, a pyridyl group which may carry a carboxyl substituent, or an amino group, or (b) the group -SO2R2 in which R2 represents a phenyl or tolyl group), and pharmaceutical compositions containing them and a non-toxic carrier, and the preparation of the esters by the processes of the examples, viz. reacting 1-(4-acetyl-1-naphthoxy)-propan-2-ol with an appropriate acid halide or anhydride, or, when R is to be -CONH2, with phosgene followed by reaction of the product with ammonia. The o-sulphobenzoate is isolated in the form of its sodium salt, and the hydrochloride of the nicotinate is described. The pharmaceutical compositions are active as muscle relaxants or anticonvulsants, and may be in forms suitable for injection or for oral administration. According to the Provisional Specification, R may also represent an acyl group, not covered by the definition above, derived from one of the following acids: di- or tri-chloracetic, dimethylaminoacetic, di- or tri-methoxybenzoic, N-methyl- or N-propyl-carbamic, benzilic, furoic, palmitic, oleic or lauric; or from ethyl hydrogen succinate. Specification 969,198 is referred to.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2450560A GB973142A (en) | 1960-07-14 | 1960-07-14 | (4-acetyl-1-naphthoxy) propyl esters |
FR858078A FR1051M (en) | 1960-04-07 | 1961-04-07 | Therapeutic agents for use as muscle relaxants and anti-convulsants. |
BE602322A BE602322A (en) | 1960-04-07 | 1961-04-07 | Therapeutic agents for use as muscle relaxants and anti-convulsants. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2450560A GB973142A (en) | 1960-07-14 | 1960-07-14 | (4-acetyl-1-naphthoxy) propyl esters |
Publications (1)
Publication Number | Publication Date |
---|---|
GB973142A true GB973142A (en) | 1964-10-21 |
Family
ID=10212710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2450560A Expired GB973142A (en) | 1960-04-07 | 1960-07-14 | (4-acetyl-1-naphthoxy) propyl esters |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB973142A (en) |
-
1960
- 1960-07-14 GB GB2450560A patent/GB973142A/en not_active Expired
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