ES426306A1 - Procedimiento para la produccion de derivados de piperidi- na. - Google Patents

Procedimiento para la produccion de derivados de piperidi- na.

Info

Publication number: ES426306A1
Authority: ES; Spain
Prior art keywords: lower alkyl; formula; bromine; chlorine; sulfur
Prior art date: 1973-05-17
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

ES426306A

Other languages

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.)

Sandoz AG

Original Assignee

Sandoz 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.)

1973-05-17

Filing date

1974-05-14

Publication date

1976-09-01

1973-05-17 Priority claimed from CH705373A external-priority patent/CH580588A5/de

1973-05-17 Priority claimed from CH705173A external-priority patent/CH580587A5/de

1973-05-17 Priority claimed from CH704873A external-priority patent/CH574956A5/de

1974-05-14 Application filed by Sandoz AG filed Critical Sandoz AG

1976-09-01 Publication of ES426306A1 publication Critical patent/ES426306A1/es

Status Expired legal-status Critical Current

Links

238000004519 manufacturing process Methods 0.000 title abstract 2
238000000034 method Methods 0.000 title abstract 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical class C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title 1
125000000217 alkyl group Chemical group 0.000 abstract 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 6
229910052794 bromium Inorganic materials 0.000 abstract 6
239000000460 chlorine Chemical group 0.000 abstract 6
229910052801 chlorine Inorganic materials 0.000 abstract 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
229910052717 sulfur Inorganic materials 0.000 abstract 6
239000011593 sulfur Substances 0.000 abstract 6
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract 5
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 4
125000003545 alkoxy group Chemical group 0.000 abstract 4
125000004414 alkyl thio group Chemical group 0.000 abstract 4
229910052731 fluorine Inorganic materials 0.000 abstract 4
239000011737 fluorine Chemical group 0.000 abstract 4
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 3
125000001309 chloro group Chemical group Cl* 0.000 abstract 3
150000001875 compounds Chemical class 0.000 abstract 3
239000001257 hydrogen Substances 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
239000005977 Ethylene Substances 0.000 abstract 1
230000002378 acidificating effect Effects 0.000 abstract 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 abstract 1
150000002431 hydrogen Chemical group 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
-1 methyleneoxy, methylenethio Chemical group 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
239000001301 oxygen Substances 0.000 abstract 1
150000003053 piperidines Chemical class 0.000 abstract 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1

Landscapes

Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

ES426306A 1973-05-17 1974-05-14 Procedimiento para la produccion de derivados de piperidi- na. Expired ES426306A1 (es)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CH705373A CH580588A5 (en)	1973-05-17	1973-05-17	4-tricyclylidene-piperidines - with sedative neuroleptic, muscle-relaxant and hypnotic activity
CH705173A CH580587A5 (en)	1973-05-17	1973-05-17	4-tricyclylidene-piperidines - with sedative neuroleptic, muscle-relaxant and hypnotic activity
CH704873A CH574956A5 (en)	1973-05-17	1973-05-17	4-tricyclylidene-piperidines - with sedative neuroleptic, muscle-relaxant and hypnotic activity

Publications (1)

Publication Number	Publication Date
ES426306A1 true ES426306A1 (es)	1976-09-01

Family

ID=27175675

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES426306A Expired ES426306A1 (es)	1973-05-17	1974-05-14	Procedimiento para la produccion de derivados de piperidi- na.

Country Status (1)

Country	Link
ES (1)	ES426306A1 (es)

1974
- 1974-05-14 ES ES426306A patent/ES426306A1/es not_active Expired

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