3-[4-(4-Morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]phenol
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3-[4-(4-Morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]phenol
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CAS No:
371935-74-9
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Formula:
C19H16N4O3
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Chemical Name:
3-[4-(4-Morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]phenol
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Synonyms:
Phenol,3-[4-(4-morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]-;3-[4-(4-Morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]phenol;PI 103;PIK 103
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CAS No:
Description
PI-103 is a potent PI3K and mTOR inhibitor with IC50s of 8 nM, 88 nM, 48 nM, 150 nM, 20 nM, and 83 nM for p110α, p110β, p110δ, p110γ, mTORC1, and mTORC2. PI-103 also inhibits DNA-PK with an IC50 of 2 nM.
3-[4-(4-Morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]phenol Basic Attributes
384.821
348.36
3-[4-(4-Morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]phenol Use and Manufacturing
(50.0 mg, 144 umol) was charged in a vial and dissolved in DMF(5.0 mL). Glutaric anhydride (49.1 mg, 431 umol) was added, followed by NaH (10.0 mg, 430 umol, 3.00 equiv) and the reaction was stirred at room temperature for 6 h. Glutaric anhydride (49.1 mg, 431 umol) was added, followed by NaH (10.0 mg, 430 umol, 3.00 equiv). After 2 h, crude was purified on a reverse phase column (5-60% MeCN/water, 2% acetic acid). Pure fractions were pooled, frozen and lyophilized. 38 mg (57%) of Compound 25A was obtained as a white lyophilized powder (4.13 mins, M+H = 463).A vial was charged with A vial was charged with A vial was charged with
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3-[4-(4-Morpholinyl)pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2-yl]phenol
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