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Structure of 25888-06-6

Chemical Structure| 25888-06-6

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Product Details of [ 25888-06-6 ]

CAS No. :25888-06-6
Formula : C10H11NO
M.W : 161.20
SMILES Code : OC1=CC2=C(N(C)C(C)=C2)C=C1
MDL No. :MFCD02904781
InChI Key :XROQKUFKUWMFEY-UHFFFAOYSA-N
Pubchem ID :12537593

Safety of [ 25888-06-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 25888-06-6 ]

* 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 [ 25888-06-6 ]

[ 25888-06-6 ] Synthesis Path-Downstream   1~28

  • 1
  • [ 1210-39-5 ]
  • [ 25888-06-6 ]
  • 2,3-dimethyl-7,7-diphenyl-7H-pyrano<3,2-e>benzimidazole [ No CAS ]
  • 7
  • [ 17591-06-9 ]
  • [ 25888-06-6 ]
  • 28
  • [ 25888-06-6 ]
  • [ 196195-13-8 ]
  • 4-(1,2-dimethylindol-5-yloxy)-6-methoxy-7-(3-morpholinopropoxy)quinazoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 148 Using an analogous procedure to that described in Example 120 OR 121 PER PP, 4-chloro-6-methoxy-7-(3-morpholinopropoxy)quinazoline (160 mg, 0.48 mmol), (prepared as described for the starting material in Example 1), was reacted with 1,2-dimethyl-5-hydroxyindole (92 mg, 0.57 mol), (Tetrahedron 1994, 50, 13433), to give 4-(1,2-dimethylindol-5-yloxy)-6-methoxy-7-(3-morpholinopropoxy)quinazoline (163 mg, 74 %).1H NMR Spectrum: (DMSOd6) 1.95-2.1 (m, 2H), 2.4 (br s, 4H), 2.45 (s, 3H), 2.5 (t, 2H), 3.65 (t, 4H), 3.75 (s, 3H), 4.0 (s,3H), 4.25 (t, 2H), 6.25 (s, 1H), 6.95 (dd, 1H), 7.3 (s, 1H), 7.38 (s, 1H), 7.45 (d, 1H), 7.6 (s, 1H), 8.5 (s, 1H) MS-ESI: 463 [MH]+
 

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Related Functional Groups of
[ 25888-06-6 ]

Alcohols

Chemical Structure| 13314-85-7

A505321 [13314-85-7]

2-Methyl-1H-indol-5-ol

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Related Parent Nucleus of
[ 25888-06-6 ]

Indoles

Chemical Structure| 13314-85-7

A505321 [13314-85-7]

2-Methyl-1H-indol-5-ol

Similarity: 0.82