Avatrombopag maleate

Avatrombopag maleate Basic information
Product Name:Avatrombopag maleate
Synonyms:677007-74-8 (MALEATE) 570406-98-3 (FREE BASE);Avatrombopag Meleate;1-[3-chloro-5-[[4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)-1,3-thiazol-2-yl]carbamoyl]pyridin-2-yl]piperidine-4-carboxylic acid;Avatrombopag Maleate;Avatrombopag maleate,677007-74-8(MALEATE)570406-98-3(FREEBASE);Avatrombopag MaleateQ: What is Avatrombopag Maleate Q: What is the CAS Number of Avatrombopag Maleate;4-Piperidinecarboxylic acid, 1-[3-chloro-5-[[[4-(4-chloro-2-thienyl)-5-(4-cyclohexyl-1-piperazinyl)-2-thi azolyl]amino]carbonyl]-2-pyridinyl]-, (2Z)-2-butenedioate (1:1);Avatrombopag Dimaleate
CAS:677007-74-8
MF:C33H38Cl2N6O7S2
MW:765.72
EINECS:
Product Categories:chemical;API;677007-74-8
Mol File:677007-74-8.mol
Avatrombopag maleate Structure
Avatrombopag maleate Chemical Properties
Safety Information
MSDS Information
Avatrombopag maleate Usage And Synthesis
DescriptionAvatrombopag maleate is a thrombopoietin receptor (TPO) agonist developed by AkaRx Inc and approved by the US FDA in May 2018 as Doptelet (20mg). For the treatment of low platelet count (thrombocytopenia CIT) in adult patients with chronic liver disease (CLD) who are scheduled to undergo medical or dental surgery.
UsesAvatrombopag Maleate is the maleate salt form of avatrombopag, an orally available platelet thrombopoietin receptor (TPOR; MPL) agonist, with potential megakaryopoiesis stimulating activity.
Mechanism of actionUpon administration, Avatrombopag maleate binds to and stimulates TPOR, which may lead to the proliferation and differentiation of megakaryocytes from bone marrow progenitor cells. This increases the production of platelets and may prevent chemotherapy-induced thrombocytopenia (CIT). TPOR is a cytokine receptor and member of the hematopoietin receptor superfamily.
SynthesisThe synthesis of Avatrombopag maleate is as follows:
A mixture containing 80.1 g of 1-(3-chloro-5-{[4-(4-chlorothiophen-2-yl)-5-(4-cyclohexyl piperazin-1-yl) thiazol-2-yl] carbamoyl} pyridin-2-yl) piperidine-4-carboxylic acid, 580 mL of DMSO, 580 mL of acetone, 17.2 g of maleic acid, and 290 mL of water was stirred at 69 °C. The insoluble matter was filtered out, washed with a mixture of 32 mL of DMSO, 32 mL of acetone, and 16 mL of water, and then the filtrate was cooled and the precipitate was collected by filtering. Washing was successively performed using 150 mL of water, 80 mL of acetone, 650 mL of water, and 80 mL of acetone, followed by drying, to obtain 70.66 g of Avatrombopag maleate.
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Avatrombopag maleate Preparation Products And Raw materials
4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amine methyl 3'-amino-2'-hydroxy-[1,1'-biphenyl]-3-carboxylate BIS(TRIMETHYLSILYL) MALONATE Lusutrombopag Ibopamine Hydrochloride Lusutrombopag Eltrombopag Avatrombopag Unii-4U07F515lg

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