ES257725A1 - Procedimiento para la preparacion de nuevos derivados de la isoindolina - Google Patents

Procedimiento para la preparacion de nuevos derivados de la isoindolina

Info

Publication number: ES257725A1
Authority: ES; Spain
Prior art keywords: general formula; hal; compounds; substituted; halogeno
Prior art date: 1959-04-30
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

ES0257725A

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.)

1959-04-30

Filing date

1960-04-29

Publication date

1960-12-01

1960-04-29 Application filed by JR Geigy AG filed Critical JR Geigy AG

1960-12-01 Publication of ES257725A1 publication Critical patent/ES257725A1/es

Status Expired legal-status Critical Current

Links

GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical class C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 title abstract 7
150000001875 compounds Chemical class 0.000 abstract 8
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 6
125000000217 alkyl group Chemical group 0.000 abstract 5
239000002253 acid Substances 0.000 abstract 3
229910021529 ammonia Inorganic materials 0.000 abstract 3
229910052739 hydrogen Inorganic materials 0.000 abstract 3
239000001257 hydrogen Substances 0.000 abstract 3
150000002596 lactones Chemical class 0.000 abstract 3
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 2
150000001412 amines Chemical class 0.000 abstract 2
239000011230 binding agent Substances 0.000 abstract 2
ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 abstract 2
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
-1 phthalic acid ester halides Chemical class 0.000 abstract 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 abstract 1
125000003545 alkoxy group Chemical group 0.000 abstract 1
125000003282 alkyl amino group Chemical group 0.000 abstract 1
150000001555 benzenes Chemical class 0.000 abstract 1
239000012965 benzophenone Substances 0.000 abstract 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
229910052794 bromium Inorganic materials 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
239000000460 chlorine Substances 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
150000001879 copper Chemical class 0.000 abstract 1
QTMDXZNDVAMKGV-UHFFFAOYSA-L copper(II) bromide Substances [Cu+2].[Br-].[Br-] QTMDXZNDVAMKGV-UHFFFAOYSA-L 0.000 abstract 1
229960003280 cupric chloride Drugs 0.000 abstract 1
125000004663 dialkyl amino group Chemical group 0.000 abstract 1
239000012954 diazonium Substances 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
125000005843 halogen group Chemical group 0.000 abstract 1
150000002367 halogens Chemical group 0.000 abstract 1
150000002431 hydrogen Chemical group 0.000 abstract 1
239000012433 hydrogen halide Substances 0.000 abstract 1
229910000039 hydrogen halide Inorganic materials 0.000 abstract 1
229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
239000011707 mineral Substances 0.000 abstract 1
150000007522 mineralic acids Chemical class 0.000 abstract 1
230000000802 nitrating effect Effects 0.000 abstract 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract 1
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 1
LGRFSURHDFAFJT-UHFFFAOYSA-N phthalic anhydride Chemical class C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
235000010269 sulphur dioxide Nutrition 0.000 abstract 1
239000004291 sulphur dioxide Substances 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Indole Compounds (AREA)

ES0257725A 1959-04-30 1960-04-29 Procedimiento para la preparacion de nuevos derivados de la isoindolina Expired ES257725A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH7277259A CH374067A (de)	1959-04-30	1959-04-30	Verfahren zur Herstellung von neuen Isoindolinderivaten

Publications (1)

Publication Number	Publication Date
ES257725A1 true ES257725A1 (es)	1960-12-01

Family

ID=4532075

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0257725A Expired ES257725A1 (es)	1959-04-30	1960-04-29	Procedimiento para la preparacion de nuevos derivados de la isoindolina

Country Status (5)

Country	Link
BE (1)	BE590329A (de)
CH (1)	CH374067A (de)
DE (1)	DE1161272B (de)
ES (1)	ES257725A1 (de)
GB (1)	GB914613A (de)

1959
- 1959-04-30 CH CH7277259A patent/CH374067A/de unknown
1960
- 1960-04-29 BE BE590329A patent/BE590329A/fr unknown
- 1960-04-29 DE DE1960G0029572 patent/DE1161272B/de active Pending
- 1960-04-29 GB GB15066/60A patent/GB914613A/en not_active Expired
- 1960-04-29 ES ES0257725A patent/ES257725A1/es not_active Expired

Also Published As

Publication number	Publication date
CH374067A (de)	1963-12-31
GB914613A (en)	1963-01-02
BE590329A (fr)	1960-10-31
DE1161272B (de)	1964-01-16

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