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5-(2-氟苯基)吡咯-3-甲醛

5-(2-fluorophenyl)-1H-Pyrrole-3-carboxaldehyde

CAS: 881674-56-2

Molecular Formula: C11H8FNO

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  5. 5-(2-氟苯基)吡咯-3-甲醛

5-(2-氟苯基)吡咯-3-甲醛 - Names and Identifiers

Name 5-(2-fluorophenyl)-1H-Pyrrole-3-carboxaldehyde
Synonyms TAK438 Impurity 54
5-(2-Fluorophenyl)-1H-pyrrole-3-carbal...
TAK-438( Vonoprazan fumarate) intermediate 3
5-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde
5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehyde
5-(2-fluorophenyl)-1H-Pyrrole-3-carboxaldehyde
1H-Pyrrole-3-carboxaldehyde, 5-(2-fluorophenyl)-
1H-Pyrrole-3-carboxaldehyde, 5-(2-fluorophenyl)-1H-pyrrole-
1H-Pyrrole-3-carboxaldehyde, 5-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde
CAS 881674-56-2
EINECS 809-913-6

5-(2-氟苯基)吡咯-3-甲醛 - Physico-chemical Properties

Molecular FormulaC11H8FNO
Molar Mass189.19
Density1.270±0.06 g/cm3(Predicted)
Melting Point133 °C
Boling Point370.6±32.0 °C(Predicted)
Solubility Chloroform (Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly)
AppearanceSolid
ColorLight Brown to Brown
pKa14.77±0.50(Predicted)
Storage Conditionunder inert gas (nitrogen or Argon) at 2-8°C
StabilityHygroscopic

5-(2-氟苯基)吡咯-3-甲醛 - Reference Information

Use 5-(2-fluorophenyl)-1H-pyrrol-3-carbaldehyde acts as a potassium competitive acid blocker (P-CAB) in the synthesis of pyrrole derivatives.
potassium competitive acid blockers for the treatment of acid-related diseases, such as gastric ulcer, duodenal ulcer, reflux esophagitis
Application 5-(2-fluorophenyl)-1H-pyrrol-3-carboxaldehyde (1-[(2S)-2-pyrrolidinecarbonyl]-pyrrolidine) is a potassium competitive acid blocker for the treatment of acid-related diseases, gastric ulcers, duodenal ulcer, reflux esophagitis, etc.
preparation with 1H pyrrole as raw material, after protection by N-alkylation of triisopropylchlorosilane, 3-aldehyde-1-H pyrrole was obtained by the reaction with the villsmeier reagent and then N-bromosuccinimide (NBS). Bromination and 2-fluorophenylboronic acid were carried out Suzuki coupling reaction to obtain 5-(2-fluorophenyl) pyrrol-3-carboxaldehyde crude product, which was refined with toluene. The overall yield was 35.5%.
Last Update:2024-04-09 19:05:15
5-(2-氟苯基)吡咯-3-甲醛
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View History
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