Berotralstat CAS 1809010-50-1

Introduction：Basic information about Berotralstat CAS 1809010-50-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Berotralstat Basic information

• Product Name: Berotralstat
• Synonyms: Berotralstat;Berotralstat (BCX-7353);1H-Pyrazole-5-carboxamide, 1-[3-(aminomethyl)phenyl]-N-[5-[(R)-(3-cyanophenyl)[(cyclopropylmethyl)amino]methyl]-2-fluorophenyl]-3-(trifluoromethyl)-;Berotralstat (BCX7353, BCX-7353);(R)-1-(3-(Aminomethyl)phenyl)-N-(5-((3-cyanophenyl)((cyclopropylmethyl)amino)methyl)-2-fluorophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide;Berotralstat Crude
• CAS: 1809010-50-1
• MF: C30H26F4N6O
• MW: 562.56
• Mol File: 1809010-50-1.mol

Berotralstat Chemical Properties

• Boiling point: 621.2±55.0 °C(Predicted)
• density: 1.38±0.1 g/cm3(Predicted)
• form: Solid
• pka: 11.33±0.70(Predicted)
• color: White to off-white

Berotralstat Usage And Synthesis

Description

Berotralstat (BCX7353, discovered by BioCryst Pharmaceuticals using a structure-guided drug design strategy) is a synthetic plasma kallikrein inhibitor that is potent and highly selective over other structurally related serine proteases.

Uses

Berotralstat is an oral plasma kallikrein inhibitor BCX7353 for treatment of hereditary angioedema.

Synthesis Reference(s)

[1] GRAS J. Berotralstat. Plasma kallikrein (KLKB1) inhibitor, Treatment of hereditary angioedema attacks[J]. Drugs of The Future, 2021, 54 1: 21. DOI:10.1358/DOF.2021.46.1.3220730.

Synthesis

Berotralstat (BCX-7353) can be prepared by Grignard reaction of magnesium [3-[bis(trimethylsilyl) amino]-4-fluorophenyl](bromido)magnesium with 3-formylbenzonitrile in THF to give secondary alcohol , which is condensed with Boc-protected acid in the presence of PyBrop and DIEA in DMF to yield the corre sponding amide. Chlorination of alcohol with SOCl2 in CH2Cl2, followed by condensation with cyclopropylmethan amine in acetonitrile at 70 °C affords secondary amine, which is N-deprotected with HCl in dioxane to yield racemic berotralstat. Resolution of racemate by preparative SFC gives (R)-berotralstat.