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Risdiplam

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CAS:1825352-65-5
Purity:99% Package:10g
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CAS:1825352-65-5
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CAS:1825352-65-5
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CAS:1825352-65-5
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CAS:1825352-65-5
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Risdiplam manufacturers

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  • 2025-05-29
  • CAS:1825352-65-5
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  • Purity: 99.43%
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  • 2025-04-05
  • CAS:1825352-65-5
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  • 2025-04-03
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Related articles

  • How is Risdiplam synthesised?
  • Risdiplam was approved by the USFDA for the treatment of spinal muscular atrophy caused by a mutation leading to a deficiency ....
  • Dec 28,2023
Risdiplam Basic information
Product Name:Risdiplam
Synonyms:7-amino-2,3-dihydro-1H-inden-4-ol;Risdiplam;RO7034067;4H-Pyrido[1,2-a]pyrimidin-4-one, 7-(4,7-diazaspiro[2.5]oct-7-yl)-2-(2,8-dimethylimidazo[1,2-b]pyridazin-6-yl)-;Risdiplam (RG-7916, RO-7034067);RG7916;2-(2,8-dimethylimidazo[1,2-b]pyridazin-6-yl)-7-(4,7-diazaspiro[2.5]octan-7-yl)-4H-pyrido[1,2-a]pyrimidin-4-one;2H4]-Risdiplam
CAS:1825352-65-5
MF:C22H23N7O
MW:401.46
EINECS:218-362-5
Product Categories:API
Mol File:1825352-65-5.mol
Risdiplam Structure
Risdiplam Chemical Properties
density 1.50±0.1 g/cm3(Predicted)
solubility Soluble in DMSO
pka9.41±0.20(Predicted)
form solid
color Light yellow to yellow
InChIInChI=1S/C22H23N7O/c1-14-9-18(26-29-11-15(2)24-21(14)29)17-10-20(30)28-12-16(3-4-19(28)25-17)27-8-7-23-22(13-27)5-6-22/h3-4,9-12,23H,5-8,13H2,1-2H3
InChIKeyASKZRYGFUPSJPN-UHFFFAOYSA-N
SMILESC12C=CC(N3CC4(CC4)NCC3)=CN1C(=O)C=C(C1=NN3C=C(C)N=C3C(C)=C1)N=2
Safety Information
MSDS Information
Risdiplam Usage And Synthesis
DescriptionRisdiplam is a survival of motor neuron 2 (SMN2) splicing modifier.
Chemical Propertieslight yellow powder to yellow powder
UsesRisdiplam is used in preparation of Imidazopyridazinyl Pyridopyrimidinones for treating spinal muscular atrophy. Gene splicing modulator.
Mechanism of actionRisdiplam works by modifying the splicing process of the SMN2 gene, increasing the production of full-length and functional SMN protein.
Side effectsBody aches or pain, chest pain or tightness, chills, cough, ear congestion, fever, headache, loss of voice, runny or stuffy nose, sneezing, sore throat, trouble breathing, unusual tiredness or weakness and so on.
SynthesisSNAr reaction between amine 194 and bromopyridine 195 gave 196 in good yield. Reduction by hydrogenation in the presence of a platinum catalyst followed by treatment with di-tert-butyl malonate gave pyridopyrimidone 197 in benzoxazole at elevated temperature in good overall yield for both steps. Mesylation to form sulfonate 198 then participated in a Suzuki coupling with 200 (derived from aryl chloride 199 via Miyaura coupling) to establish the risdiplam core skeleton. N-Boc deprotection of 201 using hydrochloric acid in isopropanol gave risdiplam (XXVI) which was isolated after pH adjustment.
Risdiplam synthesis
storage0-4℃ for short term (days to weeks) or -20℃ for long term (months)
Risdiplam Preparation Products And Raw materials
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