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Chemical Structure| 169194-80-3 Chemical Structure| 169194-80-3

Structure of 169194-80-3

Chemical Structure| 169194-80-3

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Product Details of [ 169194-80-3 ]

CAS No. :169194-80-3
Formula : C10H18N2
M.W : 166.26
SMILES Code : CC(N1CCN(C)CC1)(C)C#C
MDL No. :MFCD19687111

Safety of [ 169194-80-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H335-H314-H227
Precautionary Statements:P210-P260-P264-P270-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P370+P378-P403+P233-P403+P235-P405-P501
Class:8
UN#:1760
Packing Group:

Application In Synthesis of [ 169194-80-3 ]

* 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 [ 169194-80-3 ]

[ 169194-80-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 169194-80-3 ]
  • [ 53449-14-2 ]
  • [ 948913-18-6 ]
YieldReaction ConditionsOperation in experiment
85 - 90% With copper(l) iodide; triethylamine;palladium diacetate; triphenylphosphine; In Isopropyl acetate; dimethyl sulfoxide; at 25℃; for 4h;Product distribution / selectivity; Example 2; PBN (199.5 g, 1.2 mol, 1.2 equiv) is dissolved in isopropyl acetate to a volume of 1 L. Compound 3 (226g, 1 mol), Pd(OAc)2 (3.37 g, 0.015 mol, 1.5 mol%), and PPh3 (7.87 g, 0.03 mol, 3 mol%) are added to the solution, followed by Et3N (2,024 g, 3 mol, 3 equiv) and dimethylsulfoxide (DMSO, 2 L). The resulting solution is stirred at 25 0C for 4 h and then poured into an aqueous diamine (TMEDA, 5% v/v). The mixture is extracted with isopropyl acetate (2 L) two times, and the combined organic phases are shed with another portion of aqueous TMEDA. The organic phase is separated and activated charcoal (25g) is added. The mixture is stirred 30 min and filtered, and the resulting solution is concentrated to dryness by rotary evaporation , and the residue is <n="15"/>recrystallized from methanol/ethyl acetate to afford product A (302 - 320 g, 85 - 90% yield) in >99% purity.
70 - 80% With triethylamine;palladium dichloride; In Isopropyl acetate; dimethyl sulfoxide; at 85℃; for 6h;Product distribution / selectivity; Example 1; PBN (199.5 g, 1.2 mol, 1.2 equiv)(l-(l, l-dimethyl-prop-2-ynyl)-4-methyl-piperazine) is dissolved in isopropyl acetate to a volume of 1 L. Compound 3 (226g, 1 mol)( 7-chloro-6- nitro-3H-quinazolin-4-one) and PdCl2 (5.32 g, 0.03 mol, 3 mol%) are added to the solution, followed by Et3N (2,024 g, 20 mol, 20 equiv) and dimethylsulfoxide (DMSO, 156.3 g, 2 mol). The resulting solution is heated to 85 0C for 6 h and then allowed to cool to ambient temperature. Water (5 L) is added, the mixture is agitated and then the phases separated. The organic phase is extracted twice with water (3 L) and the combined aqueous phases are extracted with isopropyl acetate (2 L) two times. Activated charcoal (25 g) is added to the combined organic phases, and the mixture is stirred 30 min and then filtered. The resulting solution is concentrated to dryness by rotary evaporation, and the residue is recrystallized from methanoL/ethyl acetate to afford product A (249 - 284 g, 70 - 80% yield)( 7-[3-methyl- 3-(4-methyl-piperazin-l-yl)-but-l-ynyl]-6-nitro-quinazolin-4-ol) in >99% purity.
With caesium carbonate;dichloro bis(acetonitrile) palladium(II); XPhos; In Isopropyl acetate; dimethyl sulfoxide;Product distribution / selectivity; Example 7
 

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