7-Azaindole-5-carboxaldehyde

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7-Azaindole-5-carboxaldehyde Basic information
Product Name:7-Azaindole-5-carboxaldehyde
Synonyms:7-AZAINDOLE-5-CARBOXALDEHYDE;1H-Pyrrolo[2,3-b]pyridine-5-carboxaldehyde;7-Azaindole-5-carbaldehyde;7-Azaindole-5-carbaldehyd...;7-Azaindole-5-carboxaldehyde1H-Pyrrolo[2,3-b]pyridine-5-carbaldehyde;1H-Pyrrolo[2,3-b]pyridine-5-carboxaldehyde (9CI, ACI);1H-Pyrrolo[2,3-b]pyridin-5-carbaldehyd;1H-Pyrrolo[2,3-b]pyridin-5-carbaldehyde
CAS:849067-90-9
MF:C8H6N2O
MW:146.15
EINECS:
Product Categories:
Mol File:849067-90-9.mol
7-Azaindole-5-carboxaldehyde Structure
7-Azaindole-5-carboxaldehyde Chemical Properties
Melting point 181-182°C
density 1.368±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form solid
pka13.02±0.40(Predicted)
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C8H6N2O/c11-5-6-3-7-1-2-9-8(7)10-4-6/h1-5H,(H,9,10)
InChIKeyHDANOCTXZFZIHB-UHFFFAOYSA-N
SMILESC12NC=CC1=CC(C=O)=CN=2
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
WGK Germany 3
HazardClass IRRITANT
HS Code 2933399990
Storage Class13 - Non Combustible Solids
Hazard ClassificationsEye Irrit. 2
MSDS Information
7-Azaindole-5-carboxaldehyde Usage And Synthesis
Synthesis
N,N-Dimethylformamide

68-12-2

5-Bromo-7-azaindole

183208-35-7

7-Azaindole-5-carboxaldehyde

849067-90-9

The general procedure for the synthesis of 7-azaindole-5-carbaldehyde from N,N-dimethylformamide and 5-bromo-7-azaindole was as follows: to an anhydrous THF solution (50 mL) of 5-bromo-1H-pyrrolo[2,3-b]pyridine (1.0 g, 5.0 mmol, 1.0 eq.) was slowly added, under protection of argon, at -78 °C a hexane solution of 1.6 M n-butyllithium (6.7 mL, 10.7 mmol, 2.1 eq.). The reaction mixture was stirred at -78 °C for 40 min. Subsequently, 1 mL of anhydrous DMF was added to the resulting suspension and the reaction mixture was continued to be stirred overnight at room temperature. Upon completion of the reaction, the reaction mixture was quenched with saturated NH4Cl solution. The organic layer was separated and the aqueous phase was extracted with EtOAc. The organic layers were combined, washed with brine, dried over Na2SO4, filtered and concentrated to afford 1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde (Intermediate 3a) as a yellow solid (1.0 g; yield: 69%; UPLC purity: 98%).

References[1] Patent: US2018/179199, 2018, A1. Location in patent: Paragraph 0459-0460
[2] Patent: WO2016/114816, 2016, A1. Location in patent: Paragraph 0300
7-Azaindole-5-carboxaldehyde Preparation Products And Raw materials
Raw materialsMethyl formate-->N,N-Dimethylformamide-->5-Bromo-7-azaindole-->Hexane-->n-Butyllithium-->Tetrahydrofuran
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