ChemicalBook--->CAS DataBase List--->34846-65-6

34846-65-6

34846-65-6 Structure

34846-65-6 Structure
IdentificationBack Directory
[Name]

ISOQUINOLINE-4-CARBONITRILE
[CAS]

34846-65-6
[Synonyms]

ine-4-carbonitriL
4-Cyanoisoquinoline
4-Isoquinolinecarbonitrile
ISOQUINOLINE-4-CARBONITRILE
4-Cyanoisoquinoline, 4-Cyano-2-azanaphthalene
ISOQUINOLINE-4-CARBONITRILE ISO 9001:2015 REACH
[Molecular Formula]

C10H6N2
[MDL Number]

MFCD00957039
[MOL File]

34846-65-6.mol
[Molecular Weight]

154.17
Chemical PropertiesBack Directory
[Melting point ]

104 °C
[Boiling point ]

329.1±15.0 °C(Predicted)
[density ]

1.21±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

1.96±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C10H6N2/c11-5-9-7-12-6-8-3-1-2-4-10(8)9/h1-4,6-7H
[InChIKey]

NPDZTCFGRSYTPF-UHFFFAOYSA-N
[SMILES]

C1C2=C(C=CC=C2)C(C#N)=CN=1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P312-P260-P280
[HS Code ]

2933499090
Spectrum DetailBack Directory
[Spectrum Detail]

ISOQUINOLINE-4-CARBONITRILE(34846-65-6)IR1
Hazard InformationBack Directory
[Synthesis]

ZINC CYANIDE

557-21-1

3-BROMOISOQUINOLINE

34784-02-6

ISOQUINOLINE-4-CARBONITRILE

34846-65-6

To a stirred solution of 3-bromoisoquinoline (Intermediate-12) (9.2 g, 44.2 mmol) in N,N-dimethylformamide (DMF) (15 mL) was sequentially added tetrakis(triphenylphosphine)palladium (Pd(PPh3)4) (10.2 g, 8.84 mmol) and zinc cyanide (Zn(CN)2) (10.34 g, 88.44 mmol. 2.0 equiv). The reaction system was degassed with nitrogen (N2) for 20 min to exclude oxygen. Subsequently, the reaction mixture was heated to 120 °C and the reaction was stirred at this temperature overnight. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was cooled to room temperature. Insoluble impurities were removed by filtration and the filtrate was concentrated under reduced pressure to remove solvent. The resulting crude product was purified by fast column chromatography (eluent: 10% ethyl acetate/hexane) to afford the target compound 4-cyanoisoquinoline (3.4 g, 27.4% yield) as a pale yellow solid.

[References]

[1] Patent: US2013/178457, 2013, A1. Location in patent: Paragraph 0220
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