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3-isoquinolinecarboxaldehyde

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CAS:5470-80-4
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CAS:5470-80-4
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Products Intro: Product Name:Isoquinoline-3-carbaldehyde
CAS:5470-80-4

3-isoquinolinecarboxaldehyde manufacturers

3-isoquinolinecarboxaldehyde Basic information
Product Name:3-isoquinolinecarboxaldehyde
Synonyms:3-isoquinolinecarboxaldehyde;3-Formylisoquinoline;Isoquinoline-3-carboxaldehyde;3-Formylisoquinoline, 3-Formyl-2-azanaphthalene;Isoquinoline-3-carboxaldehyde 95%;3-isoquinolinecarboxaldehyde ISO 9001:2015 REACH;3-Isoquinolinecarboxaldehyde (6CI, 7CI, 8CI, 9CI, ACI);isoquinoline-3-methylaldehyde
CAS:5470-80-4
MF:C10H7NO
MW:157.17
EINECS:
Product Categories:Building Blocks;Isoquinoline;Isoquinoline Derivertives
Mol File:5470-80-4.mol
3-isoquinolinecarboxaldehyde Structure
3-isoquinolinecarboxaldehyde Chemical Properties
Melting point 47 °C
Boiling point 151 °C(Press: 10 Torr)
density 1.223±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form solid
pka2.94±0.30(Predicted)
color White
InChIInChI=1S/C10H7NO/c12-7-10-5-8-3-1-2-4-9(8)6-11-10/h1-7H
InChIKeyXOYMAJLARWXZBA-UHFFFAOYSA-N
SMILESC1C2=C(C=CC=C2)C=C(C=O)N=1
Safety Information
HS Code 2933499090
MSDS Information
3-isoquinolinecarboxaldehyde Usage And Synthesis
Synthesis Reference(s)Journal of the American Chemical Society, 73, p. 688, 1951 DOI: 10.1021/ja01146a055
Synthesis
Methyl 3-isoquinolinecarboxylate

27104-73-0

3-isoquinolinecarboxaldehyde

5470-80-4

General procedure for the synthesis of isoquinoline-3-carbaldehyde from methyl isoquinoline-3-carboxylate: methyl isoquinoline-3-carboxylate (2.0 g, 10.7 mmol) was dissolved in toluene and the solution was cooled to -78 °C. Diisobutylaluminum hydride (1 M solution in toluene, 21.4 mL, 21.4 mmol) was slowly added to this solution using a syringe over a period of 15 minutes. Keeping the reaction mixture at -78 °C, the reaction was quenched with a mixture of ether (80 mL), acetic acid (20 mL) and water (8 mL). The mixture was then slowly warmed to room temperature and stirred overnight. The organic layer was separated and the solvent was evaporated. Purification by fast column chromatography (eluent gradient: 1:4 ethyl acetate/hexane to 1:3 ethyl acetate/hexane) afforded 1.1 g of the title compound isoquinoline-3-carbaldehyde in 65% yield.1H-NMR (CDCl3, 300 MHz) δ 10.24 (s, 1H), 9.35 (s, 1H), 8.36 (s, 1H), 8.07- 7.98 (m, 2H), 7.82-7.32 (m, 2H). MS: m/z 158 ([MH]+).

References[1] Patent: WO2005/56550, 2005, A2. Location in patent: Page/Page column 75-76
[2] Patent: WO2005/92885, 2005, A1. Location in patent: Page/Page column 73
[3] Patent: WO2005/56562, 2005, A1. Location in patent: Page/Page column 71-72
[4] Tetrahedron Letters, 1999, vol. 40, # 6, p. 1211 - 1214
[5] Patent: US5554620, 1996, A
3-isoquinolinecarboxaldehyde Preparation Products And Raw materials
Raw materialsMethyl 3-isoquinolinecarboxylate-->Diethyl ether-->Toluene-->Water-->Acetic acid-->Diisobutylaluminium hydride
Tag:3-isoquinolinecarboxaldehyde(5470-80-4) Related Product Information
ISOQUINOLINE-3-CARBOXYLIC ACID Methyl 3-isoquinolinecarboxylate Isoquinoline-1-carboxylic acid 5-HYDROXYMETHYLISOQUINOLINE 1-ISOQUINOLINEMETHANOL 6-Isoquinolinecarboxaldehyde (9CI) ISOQUINOLINE N-OXIDE ISOQUINOLINE-1-CARBALDEHYDE 8-Isoquinolinecarbonitrile(9CI) ISOQUINOLINE-1-CARBOXYLIC ACID METHYL ESTER ETHYL ISOQUINOLINE-3-CARBOXYLATE Isoquinoline-3-carboxylic acid ISOQUINOLINE-5-CARBOXYLIC ACID 7-Isoquinolinecarboxaldehyde (6CI,9CI) p-[2-(3,4-dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isoquinolyl)ethyl]benzenesulphonamide 7-isoquinolinecarboxylic acid ISOQUINOLINE-5-CARBALDEHYDE QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE