SU493062A3 - Способ получени производных алканоламина - Google Patents

Способ получени производных алканоламина

Info

Publication number: SU493062A3
Authority: SU; USSR - Soviet Union
Prior art keywords: carbon atoms; alkyl; solution; derivatives; formula
Prior art date: 1969-02-21

Application number

SU1689989A

Other languages

English (en)

Russian (ru)

Inventor

Мичел Баррет Артур

Картер Джон

Халл Рой

Джеймс Ле Каунт Давид

Джон Сквайер Кристофер

Original Assignee

Империал Кемикал Индастриз Лимитед (Фирма)

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.)

1969-02-21

Filing date

1970-02-20

Publication date

1975-11-25

1969-02-21 Priority claimed from GB47048/69A external-priority patent/GB1285038A/en

1970-02-20 Application filed by Империал Кемикал Индастриз Лимитед (Фирма) filed Critical Империал Кемикал Индастриз Лимитед (Фирма)

1975-11-25 Application granted granted Critical

1975-11-25 Publication of SU493062A3 publication Critical patent/SU493062A3/ru

Links

238000004519 manufacturing process Methods 0.000 title description 2
125000004432 carbon atom Chemical group C* 0.000 description 11
239000000243 solution Substances 0.000 description 10
125000000217 alkyl group Chemical group 0.000 description 9
150000001875 compounds Chemical class 0.000 description 8
-1 nitro, hydroxy Chemical group 0.000 description 8
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 5
238000000034 method Methods 0.000 description 5
KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
125000003342 alkenyl group Chemical group 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
125000003277 amino group Chemical group 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
230000003993 interaction Effects 0.000 description 3
125000005429 oxyalkyl group Chemical group 0.000 description 3
239000007787 solid Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000000203 mixture Substances 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical class C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 1
DNSXSXYVJDPKAQ-UHFFFAOYSA-N 3-phenoxy-1-(propan-2-ylamino)butan-2-ol Chemical compound CC(C(CNC(C)C)O)OC1=CC=CC=C1 DNSXSXYVJDPKAQ-UHFFFAOYSA-N 0.000 description 1
241000337911 Copium Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
241000581652 Hagenia abyssinica Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
125000004450 alkenylene group Chemical group 0.000 description 1
125000003302 alkenyloxy group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000005160 aryl oxy alkyl group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000002026 chloroform extract Substances 0.000 description 1
150000001860 citric acid derivatives Chemical class 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000003893 lactate salts Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000003891 oxalate salts Chemical class 0.000 description 1
125000005702 oxyalkylene group Chemical group 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000001294 propane Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/22—Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C243/30—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
- C07C243/32—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton the carbon skeleton containing rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/54—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of compounds containing doubly bound oxygen atoms, e.g. esters
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/62—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by hydrogenation of carbon-to-carbon double or triple bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C07C45/74—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with dehydration
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/42—Unsaturated compounds containing hydroxy or O-metal groups
- C07C59/52—Unsaturated compounds containing hydroxy or O-metal groups a hydroxy or O-metal group being bound to a carbon atom of a six-membered aromatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/42—Unsaturated compounds containing hydroxy or O-metal groups
- C07C59/56—Unsaturated compounds containing hydroxy or O-metal groups containing halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D263/06—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by oxygen atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/24—Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

SU1689989A 1969-02-21 1970-02-20 Способ получени производных алканоламина SU493062A3 (ru)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB944569		1969-02-21
GB47048/69A GB1285038A (en)	1969-02-21	1969-02-21	Alkanolamine derivatives

Publications (1)

Publication Number	Publication Date
SU493062A3 true SU493062A3 (ru)	1975-11-25

Family

ID=26242944

Family Applications (3)

Application Number	Title	Priority Date	Filing Date
SU1689989A SU493062A3 (ru)	1969-02-21	1970-02-20	Способ получени производных алканоламина
SU701404586K SU482943A3 (ru)	1969-02-21	1970-02-20	Способ получени производных алканоламина
SU1690969A SU537626A3 (ru)	1969-02-21	1971-08-03	Способ получени производных алканоламина

Family Applications After (2)

Application Number	Title	Priority Date	Filing Date
SU701404586K SU482943A3 (ru)	1969-02-21	1970-02-20	Способ получени производных алканоламина
SU1690969A SU537626A3 (ru)	1969-02-21	1971-08-03	Способ получени производных алканоламина

Country Status (20)

Country	Link
JP (2)	JPS535287B1 (it)
AT (3)	AT305249B (it)
BE (1)	BE746107A (it)
CA (1)	CA945172A (it)
CH (3)	CH547257A (it)
CS (3)	CS153064B2 (it)
DE (1)	DE2007751C2 (it)
DK (1)	DK135278B (it)
ES (1)	ES376788A1 (it)
FI (1)	FI53120C (it)
FR (1)	FR2034561A1 (it)
IE (1)	IE34003B1 (it)
IL (1)	IL33931A (it)
KE (1)	KE2582A (it)
NL (1)	NL162363C (it)
NO (1)	NO128653B (it)
PL (3)	PL77781B1 (it)
SE (1)	SE391517B (it)
SU (3)	SU493062A3 (it)
YU (4)	YU34275B (it)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1311521A (en) *	1970-02-13	1973-03-28	Ici Ltd	Alkanolamine derivatives
DE2048838A1 (de) *	1970-10-05	1972-04-06	C H Boehnnger Sohn, 6507 Ingel heim	Neue 1 Phenoxy 2 hydroxy 3 hydroxyal kylaminopropane und Verfahren zu ihrer Her stellung
FR2132570B1 (it) *	1971-04-09	1974-08-02	Lipha
GB1387630A (en) *	1971-05-07	1975-03-19	Ici Ltd	Phenoxyalkanolamine derivatives
GB1433595A (en) *	1972-07-06	1976-04-28	Ici Ltd	Alkanolamine derivatives
DE2623314C2 (de) *	1976-05-25	1984-08-02	Hoechst Ag, 6230 Frankfurt	1-Aryloxy-2-Hydroxy-3-aminopropane, Verfahren zu ihrer Herstellung und diese enthaltende Arzneimittel
DE2818999A1 (de) *	1978-04-29	1979-11-15	Basf Ag	Aminoderivate von 3-alkyl-5-(2- hydroxystyryl)-isoxazolen
DE2943405A1 (de)	1979-10-26	1981-05-07	Basf Ag, 6700 Ludwigshafen	Neue aminoderivate des 5-(2-hydroxystyryl)-isoxazols
US4387103A (en) *	1980-11-28	1983-06-07	American Hospital Supply Corporation	Method for treatment or prophylaxis of cardiac disorders
US4593119A (en) *	1980-11-28	1986-06-03	American Hospital Supply Corporation	Method for treatment or prophylaxis of cardiac disorders
JPS57105206U (it) *	1980-12-16	1982-06-29
DE3407695A1 (de) *	1984-03-02	1985-09-12	Röhm Pharma GmbH, 6108 Weiterstadt	Pteridinverbindungen mit pharmazeutischer wirksamkeit
DE3500761A1 (de) *	1985-01-11	1986-09-04	SOUR "PODRAVKA" OOUR "BELUPO 2", Proizvodnja kozmeti&ccaron;kih preparata i lijekova, Koprivnica	Verfahren zur gewinnung von atenolol und seiner derivate
US4971959A (en) *	1987-04-14	1990-11-20	Warner-Lambert Company	Trisubstituted phenyl analogs having activity for congestive heart failure
EP0673924A4 (en) *	1992-12-10	1996-04-24	Teikoku Chem Ind Co Ltd	PROPRIONIC ACID DERIVATIVE.
WO1998048787A1 (en) *	1997-04-30	1998-11-05	Eli Lilly And Company	INTERMEDIATES AND A PROCESS FOR PREPARING BENZO[b]THIOPHENES
JP5225574B2 (ja) *	2006-11-09	2013-07-03	エムキュアファーマシューティカルズリミテッド	β遮断薬化合物の改善された調製方法
WO2010079497A2 (en)	2009-01-12	2010-07-15	Hetero Research Foundation	Novel polymorph of atazanavir sulfate

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1593762A1 (de) *	1967-02-06	1972-06-08	Boehringer Sohn Ingelheim	Verfahren zur Herstellung von neuen substituierten 1-Phenoxy-2-hydroxy-3-alkylaminopropanen

1970
- 1970-02-09 CA CA074,353A patent/CA945172A/en not_active Expired
- 1970-02-10 IE IE174/70A patent/IE34003B1/xx unknown
- 1970-02-11 PL PL1970138762A patent/PL77781B1/pl unknown
- 1970-02-11 PL PL1970174450A patent/PL87019B1/pl unknown
- 1970-02-11 PL PL1970174445A patent/PL93998B1/pl unknown
- 1970-02-17 BE BE746107D patent/BE746107A/xx not_active IP Right Cessation
- 1970-02-18 AT AT762071A patent/AT305249B/de not_active IP Right Cessation
- 1970-02-18 AT AT761571A patent/AT305244B/de not_active IP Right Cessation
- 1970-02-18 CH CH232770A patent/CH547257A/xx not_active IP Right Cessation
- 1970-02-18 AT AT146270A patent/AT303005B/de not_active IP Right Cessation
- 1970-02-18 CH CH1804972A patent/CH561175A5/xx not_active IP Right Cessation
- 1970-02-18 CH CH1804472A patent/CH553747A/xx not_active IP Right Cessation
- 1970-02-19 DK DK81370AA patent/DK135278B/da unknown
- 1970-02-19 DE DE2007751A patent/DE2007751C2/de not_active Expired
- 1970-02-19 YU YU410/70A patent/YU34275B/xx unknown
- 1970-02-19 IL IL33931A patent/IL33931A/xx unknown
- 1970-02-19 FI FI443/70A patent/FI53120C/fi active
- 1970-02-20 CS CS561270*A patent/CS153064B2/cs unknown
- 1970-02-20 CS CS118670A patent/CS153062B2/cs unknown
- 1970-02-20 SU SU1689989A patent/SU493062A3/ru active
- 1970-02-20 SU SU701404586K patent/SU482943A3/ru active
- 1970-02-20 FR FR7006241A patent/FR2034561A1/fr active Granted
- 1970-02-20 JP JP1473970A patent/JPS535287B1/ja active Pending
- 1970-02-20 CS CS561770*A patent/CS153069B2/cs unknown
- 1970-02-20 NO NO00611/70A patent/NO128653B/no unknown
- 1970-02-20 SE SE7002190A patent/SE391517B/xx unknown
- 1970-02-20 NL NL7002414.A patent/NL162363C/xx not_active IP Right Cessation
- 1970-02-21 ES ES376788A patent/ES376788A1/es not_active Expired
1971
- 1971-08-03 SU SU1690969A patent/SU537626A3/ru active
1973
- 1973-01-18 JP JP48008227A patent/JPS5037182B1/ja active Pending
1975
- 1975-06-29 YU YU1933/75A patent/YU34278B/xx unknown
- 1975-07-29 YU YU1936/75A patent/YU34281B/xx unknown
- 1975-07-29 YU YU1934/75A patent/YU34279B/xx unknown
- 1975-11-24 KE KE2582*UA patent/KE2582A/xx unknown

Also Published As

Publication number	Publication date
FR2034561B1 (it)	1974-05-24
IL33931A (en)	1974-01-14
IL33931A0 (en)	1970-04-20
ES376788A1 (es)	1972-09-16
AT303005B (de)	1972-11-10
YU193375A (en)	1978-10-31
SU537626A3 (ru)	1976-11-30
PL87019B1 (en)	1976-06-30
DE2007751C2 (de)	1983-12-15
YU41070A (en)	1978-10-31
DK135278C (it)	1977-09-12
CS153062B2 (it)	1974-02-22
FR2034561A1 (en)	1970-12-11
YU193675A (en)	1978-10-31
DE2007751A1 (it)	1970-09-10
CH547257A (de)	1974-03-29
IE34003L (en)	1970-08-21
YU34281B (en)	1979-04-30
JPS535287B1 (it)	1978-02-25
BE746107A (fr)	1970-08-17
NO128653B (it)	1973-12-27
NL162363C (nl)	1980-05-16
YU34278B (en)	1979-04-30
SE391517B (sv)	1977-02-21
YU34279B (en)	1979-04-30
CA945172A (en)	1974-04-09
FI53120B (it)	1977-10-31
CS153069B2 (it)	1974-02-22
CH561175A5 (it)	1975-04-30
IE34003B1 (en)	1975-01-08
JPS5037182B1 (it)	1975-12-01
YU193475A (en)	1978-10-31
AT305249B (de)	1973-02-12
NL162363B (nl)	1979-12-17
DK135278B (da)	1977-03-28
FI53120C (it)	1978-02-10
CS153064B2 (en)	1974-02-22
SU482943A3 (ru)	1975-08-30
PL93998B1 (en)	1977-07-30
NL7002414A (it)	1970-08-25
KE2582A (en)	1975-12-05
PL77781B1 (en)	1975-04-30
YU34275B (en)	1979-04-30
CH553747A (de)	1974-09-13
AT305244B (de)	1973-02-12

Publication	Publication Date	Title
BG60270B1 (bg)	1994-03-31	Метод за получаване на 5н-2,3-бензодиазепинови производни
SU537626A3 (ru)	1976-11-30	Способ получени производных алканоламина
Hall et al.	1940	Syntheses in the pyrazine series. II. Preparation and properties of aminopyrazine
Parham et al.	1950	Reactions of diazo compounds with nitroölefins. I. The preparation of pyrazoles
SU443509A1 (ru)	1974-09-15	Способ получени производных бензола или их солей
Adams et al.	1949	Leucenol. VI. A total synthesis
SU433680A3 (it)	1974-06-25
Heymann et al.	1945	Derivatives of p, p'-Diaminodiphenyl Sulfone1a
Rodionow	1929	Synthesis of beta-aryl-beta-amino-ethane-alpha, alpha-dicarbonic acids the mechanism of Knoevenagel's synthesis of cinnamic acids
Elvidge et al.	1960	343. 1, 4-Dimethoxyphthalazine and the other O-and N-methyl derivatives of phthalhydrazide
SU492076A3 (ru)	1975-11-15	Способ получени замещенных гуанидина
US3833608A (en)	1974-09-03	Indole-3-methanesulfonamides
SU432718A3 (ru)	1974-06-15	Способ получения2-замещенных производных1-циннамилбензимидазола
FI60863B (fi)	1981-12-31	Foerfarande foer framstaellning av nya bentshydryloxialkylaminderivat med foerlaengd antihistamineffekt
US3249611A (en)	1966-05-03	Novel method for the preparation of phthalazines
GB1469197A (en)	1977-03-30	Preparation of 1-aminoalkyl triazolobenzodiazepines
US2265217A (en)	1941-12-09	D - lysergic acid -
Cromwell et al.	1956	Reactions of β-Benzoylacrylic Acid and its Methyl Ester with Hydrazines. Absorption Spectra Studies1
Scott et al.	1952	New Compounds. Some Aldehydic Hydrazones of Triaiminoguanidine
Geissman et al.	1946	THE PREPARATION OF 1, 3-DIAMINO-2-METHYLAMINOPROPANE AND 1, 3-DIAMINO-2-AMINOMETHYLPROPANE1
Funk et al.	1923	Some New Derivatives of Synthetic Adrenaline (Suprarenine)
CH587796A5 (en)	1977-05-13	2-Aminoalkyl amino indanes - anti-arrhythmic,orally active, long-acting, not myocardial depressant
Emling et al.	1949	Furfuryl and Thenylalkylamines from Schiff Bases
SU467902A1 (ru)	1975-04-25	Способ получени 2-( -нитрозамино)-бензимидазолов
Jensen et al.	1926	The synthesis of acridine-9-ethylamine