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Chemical Structure| 1415379-56-4 Chemical Structure| 1415379-56-4
Chemical Structure| 1415379-56-4

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T807 a tau positron emission tomography (PET) tracer.

Synonyms: AV-1451

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of T807

CAS No. :1415379-56-4
Formula : C16H10FN3
M.W : 263.27
SMILES Code : FC1=CC=C(C2=CC3=C(C=C2)C(C=NC=C4)=C4N3)C=N1
Synonyms :
AV-1451
English Name :7-(6-Fluoropyridin-3-yl)-5H-pyrido[4,3-b]indole
MDL No. :MFCD29767874
InChI Key :GETAAWDSFUCLBS-UHFFFAOYSA-N
Pubchem ID :71059746

Safety of T807

Application In Synthesis of T807

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1415379-56-4 ]

[ 1415379-56-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 233276-35-2 ]
  • [ 1415379-56-4 ]
  • [ 2226298-72-0 ]
YieldReaction ConditionsOperation in experiment
82% With sodium hydride In 1-methyl-pyrrolidin-2-one; mineral oil at 0 - 20℃; for 2h; 1 Step 1:
7-(6-((1s,3s)-3-(benzyloxy)cyclobutoxy)pyridin-3-yl)-5H-pyrido[4,3-b]indole
To a solution of 7-(6-fluoropyridin-3-yl)-5H-pyrido[4,3-b]indole (1.1 g, 4.18 mmol) and (1s,3s)-3-(benzyloxy)cyclobutanol (745 mg, 4.18 mmol) in 1-methylpyrrolidin-2-one (2 ml) was added sodium hydride (60% in mineral oil) (334 mg, 8.35 mmol) at 0° C. The mixture was stirred at room temperature for 2 hours. TLC showed the reaction was complete. The mixture was partitioned between ethyl acetate (20 ml) and water (20 ml). The organic layer was collected, washed with brine (30 ml), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give a crude residue which was purified by silica gel flash chromatography (eluted with 2-5% methanol in dichloromethane) to afford 7-(6-((1 s,3s)-3-(benzyloxy)cyclobutoxy)pyridin-3-yl)-5H-pyrido[4,3-b]indole (1.42 g, 82%) as white solid.
82% With sodium hydride In 1-methyl-pyrrolidin-2-one; mineral oil at 0 - 20℃; for 2h; 1 Step 1 : 7-(6-((ls,3s)-3-(benzyloxy)cyclobutoxy)pyridin-3-yl)-5H-pyrido[4,3-b]indole To a solution of 7-(6-fluoropyridin-3-yl)-5H-pyrido[4,3-b]indole (1.1 g, 4.18 mmol) and (ls,3s)-3-(benzyloxy)cyclobutanol (745 mg, 4.18 mmol) in l-methylpyrrolidin-2-one (2 ml) was added sodium hydride (60% in mineral oil) (334 mg, 8.35 mmol) at 0°C. The mixture was stirred at room temperature for 2 hours. TLC showed the reaction was complete. The mixture was partitioned between ethyl acetate (20 ml) and water (20 ml). The organic layer was collected, washed with brine (30 ml), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give a crude residue which was purified by silica gel flash chromatography (eluted with 2-5% methanol in dichloromethane) to afford 7-(6-((ls, 3 s)-3 -(benzyl oxy)cyclobutoxy)pyri din-3 - yl)-5H-pyrido[4,3-b]indole (1.42 g, 82%) as white solid.
  • 2
  • [ 1396215-84-1 ]
  • [ 1415379-56-4 ]
  • [ 3096198-56-7 ]
YieldReaction ConditionsOperation in experiment
91% With 4-(benzoyloxy)morpholine; tetrakis(actonitrile)copper(I) hexafluorophosphate; 4,7-dimethoxy-1,10-phenanthroline; 2-tert-butyl-1,1,3,3-tetramethylguanidine In acetonitrile at 60℃; for 16h; Inert atmosphere; Schlenk technique; Sealed tube;
 

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