GB1160597A – Novel Isoxazolo[5,4-6]Pyridines and the Preparation Thereof
– Google Patents
GB1160597A – Novel Isoxazolo[5,4-6]Pyridines and the Preparation Thereof
– Google Patents
Novel Isoxazolo[5,4-6]Pyridines and the Preparation Thereof
Info
Publication number
GB1160597A
GB1160597A
GB5653/67A
GB565367A
GB1160597A
GB 1160597 A
GB1160597 A
GB 1160597A
GB 5653/67 A
GB5653/67 A
GB 5653/67A
GB 565367 A
GB565367 A
GB 565367A
GB 1160597 A
GB1160597 A
GB 1160597A
Authority
GB
United Kingdom
Prior art keywords
formula
salts
compounds
contain
isoxazolo
Prior art date
1966-03-04
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
Application number
GB5653/67A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn Co
Priority date (The priority date 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 date listed.)
1966-03-04
Filing date
1967-02-06
Publication date
1969-08-06
1967-02-06
Application filed by Upjohn Co
filed
Critical
Upjohn Co
1969-08-06
Publication of GB1160597A
publication
Critical
patent/GB1160597A/en
Status
Expired
legal-status
Critical
Current
Links
Espacenet
Global Dossier
Discuss
150000003222
pyridines
Chemical class
0.000
title
1
150000001875
compounds
Chemical class
0.000
abstract
4
239000002253
acid
Substances
0.000
abstract
3
239000000203
mixture
Substances
0.000
abstract
3
150000003839
salts
Chemical class
0.000
abstract
3
239000004480
active ingredient
Substances
0.000
abstract
2
125000005036
alkoxyphenyl group
Chemical group
0.000
abstract
2
125000005037
alkyl phenyl group
Chemical group
0.000
abstract
2
125000005059
halophenyl group
Chemical group
0.000
abstract
2
230000002363
herbicidal effect
Effects
0.000
abstract
2
125000001997
phenyl group
Chemical group
[H]C1=C([H])C([H])=C(*)C([H])=C1[H]
0.000
abstract
2
YNJBWRMUSHSURL-UHFFFAOYSA-N
trichloroacetic acid
Chemical class
OC(=O)C(Cl)(Cl)Cl
YNJBWRMUSHSURL-UHFFFAOYSA-N
0.000
abstract
2
DITTYRBIXKVOTK-UHFFFAOYSA-N
[1,2]oxazolo[5,4-b]pyridine
Chemical class
C1=CC=C2C=NOC2=N1
DITTYRBIXKVOTK-UHFFFAOYSA-N
0.000
abstract
1
125000000217
alkyl group
Chemical group
0.000
abstract
1
230000000843
anti-fungal effect
Effects
0.000
abstract
1
230000003110
anti-inflammatory effect
Effects
0.000
abstract
1
239000003795
chemical substances by application
Substances
0.000
abstract
1
239000003937
drug carrier
Substances
0.000
abstract
1
229910052739
hydrogen
Inorganic materials
0.000
abstract
1
239000001257
hydrogen
Substances
0.000
abstract
1
125000004435
hydrogen atom
Chemical class
[H]*
0.000
abstract
1
239000008194
pharmaceutical composition
Substances
0.000
abstract
1
230000001225
therapeutic effect
Effects
0.000
abstract
1
Classifications
C—CHEMISTRY; METALLURGY
C07—ORGANIC CHEMISTRY
C07D—HETEROCYCLIC COMPOUNDS
C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
C07D498/04—Ortho-condensed systems
C—CHEMISTRY; METALLURGY
C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
C23G1/04—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
C23G1/06—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors
C23G1/065—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors sulfur-containing compounds
Abstract
1,160,597. Therapeutic and herbicidal compositions. UPJOHN CO. 6 Feb., 1967 [4 March, 1966], No. 5653/67. Headings A5B and A5E. [Also in Division C2] Pharmaceutical compositions, contain as the active ingredient novel isoxazolo [5, 4-b] pyridines or acid addition salts thereof of the formula I and Ia wherein R is C 1-4 alkyl, phenyl, C 1-4 alkylphenyl; C 1-4 alkoxyphenyl or halophenyl, R
GB5653/67A
1966-03-04
1967-02-06
Novel Isoxazolo[5,4-6]Pyridines and the Preparation Thereof
Expired
GB1160597A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
US53174666A
1966-03-04
1966-03-04
Publications (1)
Publication Number
Publication Date
GB1160597A
true
GB1160597A
(en)
1969-08-06
Family
ID=24118883
Family Applications (1)
Application Number
Title
Priority Date
Filing Date
GB5653/67A
Expired
GB1160597A
(en)
1966-03-04
1967-02-06
Novel Isoxazolo[5,4-6]Pyridines and the Preparation Thereof
Country Status (6)
Country
Link
US
(1)
US3541101A
(en)
DE
(1)
DE1695931A1
(en)
FR
(1)
FR1513038A
(en)
GB
(1)
GB1160597A
(en)
IL
(1)
IL27443A
(en)
NL
(1)
NL6702765A
(en)
Families Citing this family (7)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
US4179566A
(en)
*
1975-08-06
1979-12-18
Sandoz, Inc.
Substituted hydroxy pyridones
US4024262A
(en)
*
1975-08-06
1977-05-17
Sandoz, Inc.
Substituted hydroxy pyridones
AU561013B2
(en)
*
1982-03-30
1987-04-30
Gruppo Lepetit S.P.A.
Isoxazole(5,4-beta)pyridines
US4767762A
(en)
*
1985-12-23
1988-08-30
Abbott Laboratories
Tricyclic quinoline and naphthyride antibacterials
JPH02237988A
(en)
*
1988-11-18
1990-09-20
Nissan Chem Ind Ltd
Isooxazolopyridine-based mevalonolactone
CN103124733B
(en)
*
2010-07-22
2016-03-30
巴斯夫欧洲公司
Weeding isoxazole is [5,4-b] pyridine also
BR112014017209A8
(en)
2012-01-12
2017-07-04
Basf Se
compounds, composition, method for preparing a composition and method for controlling undesirable vegetation
Family Cites Families (3)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
US3005824A
(en)
*
1958-03-29
1961-10-24
Bayer Ag
8-aza-(linear naphthothiazole)-4, 9-quinones substituted in the 2-position
US3336306A
(en)
*
1965-10-22
1967-08-15
American Home Prod
Oxazoloisoindolones and related compounds
US3381016A
(en)
*
1966-03-04
1968-04-30
Upjohn Co
Isoxazolo[5, 4-b]pyridine derivatives and a method for their preparation
1966
1966-03-04
US
US531746A
patent/US3541101A/en
not_active
Expired – Lifetime
1967
1967-02-06
GB
GB5653/67A
patent/GB1160597A/en
not_active
Expired
1967-02-15
IL
IL27443A
patent/IL27443A/en
unknown
1967-02-23
NL
NL6702765A
patent/NL6702765A/xx
unknown
1967-02-24
DE
DE19671695931
patent/DE1695931A1/en
active
Pending
1967-03-03
FR
FR97358A
patent/FR1513038A/en
not_active
Expired
Also Published As
Publication number
Publication date
FR1513038A
(en)
1968-02-09
NL6702765A
(en)
1967-09-05
DE1695931A1
(en)
1971-05-06
IL27443A
(en)
1970-11-30
US3541101A
(en)
1970-11-17
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Legal Events
Date
Code
Title
Description
1969-12-17
PS
Patent sealed [section 19, patents act 1949]
1972-08-31
PLNP
Patent lapsed through nonpayment of renewal fees
