ES258418A1 - Procedimiento para la prepaarcion de nuevos derivados de iminodibencilo - Google Patents

Procedimiento para la prepaarcion de nuevos derivados de iminodibencilo

Info

Publication number: ES258418A1
Authority: ES; Spain
Prior art keywords: general formula; compounds; reacting; group; acid
Prior art date: 1959-05-28
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

ES0258418A

Other languages

English (en)

Spanish (es)

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.)

Novartis AG

Original Assignee

JR Geigy AG

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.)

1959-05-28

Filing date

1960-05-27

Publication date

1960-11-16

1960-01-29 Priority claimed from CH98160A external-priority patent/CH381692A/de

1960-01-29 Priority claimed from CH97960A external-priority patent/CH378893A/de

1960-05-27 Application filed by JR Geigy AG filed Critical JR Geigy AG

1960-11-16 Publication of ES258418A1 publication Critical patent/ES258418A1/es

Status Expired legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 abstract 17
239000002253 acid Substances 0.000 abstract 7
ZSMRRZONCYIFNB-UHFFFAOYSA-N 6,11-dihydro-5h-benzo[b][1]benzazepine Chemical group C1CC2=CC=CC=C2NC2=CC=CC=C12 ZSMRRZONCYIFNB-UHFFFAOYSA-N 0.000 abstract 5
-1 aralkyl halide Chemical class 0.000 abstract 5
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 4
150000002148 esters Chemical class 0.000 abstract 4
150000001408 amides Chemical class 0.000 abstract 3
150000001412 amines Chemical class 0.000 abstract 3
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 2
150000001339 alkali metal compounds Chemical class 0.000 abstract 2
125000003282 alkyl amino group Chemical group 0.000 abstract 2
229940100198 alkylating agent Drugs 0.000 abstract 2
239000002168 alkylating agent Substances 0.000 abstract 2
239000007864 aqueous solution Substances 0.000 abstract 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
239000011230 binding agent Substances 0.000 abstract 2
125000004432 carbon atom Chemical group C* 0.000 abstract 2
ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 abstract 2
230000003301 hydrolyzing effect Effects 0.000 abstract 2
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
150000003839 salts Chemical class 0.000 abstract 2
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 abstract 2
DWEDVKMRFXQLQH-UHFFFAOYSA-N 2-Hydroxyiminodibenzyl Chemical group C1CC2=CC(O)=CC=C2NC2=CC=CC=C21 DWEDVKMRFXQLQH-UHFFFAOYSA-N 0.000 abstract 1
BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
238000006085 Schmidt reaction Methods 0.000 abstract 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 abstract 1
238000005903 acid hydrolysis reaction Methods 0.000 abstract 1
239000003513 alkali Substances 0.000 abstract 1
229910052783 alkali metal Inorganic materials 0.000 abstract 1
150000001340 alkali metals Chemical class 0.000 abstract 1
150000003973 alkyl amines Chemical class 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 abstract 1
125000005277 alkyl imino group Chemical group 0.000 abstract 1
125000002947 alkylene group Chemical group 0.000 abstract 1
125000003277 amino group Chemical group 0.000 abstract 1
230000003266 anti-allergic effect Effects 0.000 abstract 1
230000001754 anti-pyretic effect Effects 0.000 abstract 1
239000000935 antidepressant agent Substances 0.000 abstract 1
239000002221 antipyretic Substances 0.000 abstract 1
239000011260 aqueous acid Substances 0.000 abstract 1
125000003710 aryl alkyl group Chemical group 0.000 abstract 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
150000001538 azepines Chemical class 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
150000001805 chlorine compounds Chemical class 0.000 abstract 1
239000010941 cobalt Substances 0.000 abstract 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 1
229910001429 cobalt ion Inorganic materials 0.000 abstract 1
125000004663 dialkyl amino group Chemical group 0.000 abstract 1
125000005265 dialkylamine group Chemical group 0.000 abstract 1
239000012954 diazonium Substances 0.000 abstract 1
150000001989 diazonium salts Chemical class 0.000 abstract 1
150000005690 diesters Chemical class 0.000 abstract 1
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 abstract 1
125000005670 ethenylalkyl group Chemical group 0.000 abstract 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
150000002170 ethers Chemical class 0.000 abstract 1
150000004820 halides Chemical class 0.000 abstract 1
238000010438 heat treatment Methods 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
238000007327 hydrogenolysis reaction Methods 0.000 abstract 1
230000007062 hydrolysis Effects 0.000 abstract 1
238000006460 hydrolysis reaction Methods 0.000 abstract 1
150000002440 hydroxy compounds Chemical class 0.000 abstract 1
125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
229910052742 iron Inorganic materials 0.000 abstract 1
229910001437 manganese ion Inorganic materials 0.000 abstract 1
229910052987 metal hydride Inorganic materials 0.000 abstract 1
150000004681 metal hydrides Chemical class 0.000 abstract 1
LLCOIQRNSJBFSN-UHFFFAOYSA-N methane;sulfurochloridic acid Chemical compound C.OS(Cl)(=O)=O LLCOIQRNSJBFSN-UHFFFAOYSA-N 0.000 abstract 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
150000007522 mineralic acids Chemical class 0.000 abstract 1
230000007935 neutral effect Effects 0.000 abstract 1
229910001453 nickel ion Inorganic materials 0.000 abstract 1
229910052757 nitrogen Inorganic materials 0.000 abstract 1
125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
231100000252 nontoxic Toxicity 0.000 abstract 1
230000003000 nontoxic effect Effects 0.000 abstract 1
150000007524 organic acids Chemical class 0.000 abstract 1
230000003647 oxidation Effects 0.000 abstract 1
238000007254 oxidation reaction Methods 0.000 abstract 1
230000001590 oxidative effect Effects 0.000 abstract 1
239000001301 oxygen Substances 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
125000004430 oxygen atom Chemical group O* 0.000 abstract 1
239000008194 pharmaceutical composition Substances 0.000 abstract 1
XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 abstract 1
KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 abstract 1
229910052700 potassium Inorganic materials 0.000 abstract 1
239000011591 potassium Substances 0.000 abstract 1
238000002360 preparation method Methods 0.000 abstract 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
239000000932 sedative agent Substances 0.000 abstract 1
230000001624 sedative effect Effects 0.000 abstract 1
239000000243 solution Substances 0.000 abstract 1
229960002317 succinimide Drugs 0.000 abstract 1
238000003420 transacetalization reaction Methods 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated

Landscapes

Hydrogenated Pyridines (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

ES0258418A 1959-05-28 1960-05-27 Procedimiento para la prepaarcion de nuevos derivados de iminodibencilo Expired ES258418A1 (es)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CH7368359		1959-05-28
CH98160A CH381692A (de)	1960-01-29	1960-01-29	Verfahren zur Herstellung von neuen Iminodibenzylderivaten
CH97960A CH378893A (de)	1960-01-29	1960-01-29	Verfahren zur Herstellung von neuen N-heterocyclischen Verbindungen

Publications (1)

Publication Number	Publication Date
ES258418A1 true ES258418A1 (es)	1960-11-16

Family

ID=27172570

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0258418A Expired ES258418A1 (es)	1959-05-28	1960-05-27	Procedimiento para la prepaarcion de nuevos derivados de iminodibencilo

Country Status (3)

Country	Link
BE (1)	BE591293A (fr)
ES (1)	ES258418A1 (fr)
GB (1)	GB926816A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2013078244A1 (fr)	2011-11-21	2013-05-30	Promega Corporation	Analogues de carboxy x rhodamine

1960
- 1960-05-27 ES ES0258418A patent/ES258418A1/es not_active Expired
- 1960-05-27 BE BE591293A patent/BE591293A/fr unknown
- 1960-05-30 GB GB18978/60A patent/GB926816A/en not_active Expired

Also Published As

Publication number	Publication date
BE591293A (fr)	1960-11-28
GB926816A (en)	1963-05-22

Publication	Publication Date	Title
AU528275B2 (en)	1983-04-21	Imidazole derivatives
ES8404307A1 (es)	1984-05-01	Un procedimiento para la preparacion de derivados de acidos alcanoicos.
GB1324469A (en)	1973-07-25	Derivatives of benzodiazepines
HUT70562A (en)	1995-10-30	Process for producing vitamin d-25-carboxylic acid derivatives and pharmaceutical compositions containing them
AU540916B2 (en)	1984-12-06	3,1 benzoxazin-2-ones
ATE28187T1 (de)	1987-07-15	Polyprenylcarbonsaeureamide und verfahren zu ihrer herstellung.
NZ196284A (en)	1983-12-16	1-piperazino-3-phenylindane derivatives:pharmaceutical compositions
GB1413892A (en)	1975-11-12	2-pyrimidinyl-thio-acetic acids and their derivatives
GB926816A (en)	1963-05-22	Improvements in and relating to n-heterocyclic compounds
AU9263298A (en)	1999-03-08	Phospholipid analogue compounds
ES8106289A1 (es)	1981-02-16	Procedimiento de preparacion de nuevos derivados del a-fe- nil-2-pirrolidin-metanol
ES8401068A1 (es)	1983-12-01	Procedimiento para la preparacion de derivados de corinanteina, asi como de sus sales de adicion acida fisiologicamente inocuas.
ES8106914A1 (es)	1981-10-01	Procedimiento para la preparacion de nuevos derivados de amino-14 esteroides.
ES267445A1 (es)	1961-11-16	Procedimiento para la obtenciën de nuevas n-fenil piperacinas
ES8504815A1 (es)	1985-05-01	Un procedimiento para la preparacion de nuevos derivados de penem 2-tiosustituidos
FI964410A0 (fi)	1996-11-01	Menetelmä 4-amino-delta4-3-ketosteroidien valmistamiseksi 4-nitro-delta4-3-ketosteroidien kautta
GB1412377A (en)	1975-11-05	Oxazolo- 5,4-d azepines
IL115085A (en)	1999-06-20	Piperazine bicyclic carboxamide derivatives their preparation and pharmaceutical compositions containing them
ES8105268A1 (es)	1981-06-01	Procedimiento para preparar derivados de acido acilaminoben-zoico
ATE29251T1 (de)	1987-09-15	Aminopyridincarbonsaeure-derivate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zusammensetzungen.
GB1391234A (en)	1975-04-16	Indole derivatives
JPS6461462A (en)	1989-03-08	Manufacture of acylated imidazole and pyrazole
ES8400434A1 (es)	1983-10-16	"un procedimiento para preparar 1,2-dihidropirido(3,4-b)pirazinas".
ES260973A1 (es)	1961-01-16	Procedimiento para preparar nuevos compuestos n-heterociclicos
FR2897779B1 (fr)	2009-04-17	Manossyl-1 phosphates, procede de preparation et utilisation en therapeutique, notamment vis-a-vis dy syndrome cdg-la