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Chemical Structure| 136727-12-3 Chemical Structure| 136727-12-3

Structure of 136727-12-3

Chemical Structure| 136727-12-3

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Product Details of [ 136727-12-3 ]

CAS No. :136727-12-3
Formula : C9H10N2O
M.W : 162.19
SMILES Code : CNCC1=NC2=CC=CC=C2O1
MDL No. :MFCD09038216

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Application In Synthesis of [ 136727-12-3 ]

* 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 [ 136727-12-3 ]

[ 136727-12-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 73101-74-3 ]
  • [ 136727-12-3 ]
YieldReaction ConditionsOperation in experiment
71% b 2-[(Methylamino)methyl]benzoxazole Following the procedure of Example 4(b), except using 2-bromomethyl benzoxazole in place of 2-bromomethylbenzothiazole, the title compound (0.250 g, 71%) was prepared as a brown oil: 1 H NMR (400 MHz, DMSO-d6) delta 2,75 (s, 3H), 4.71 (s, 2H), 7.60 (m, 2H), 8.01 (d, J=7.9 Hz, 1H), 8.17 (d, J=7.9 Hz, 1H).
  • 2
  • [ 41014-43-1 ]
  • [ 136727-12-3 ]
YieldReaction ConditionsOperation in experiment
3.18 g (82%) In water; methylamine; Step 2) Preparation of 2-(Methylaminomethyl)benzoxazole 2-(Chloromethyl)benzoxazole (3.99 g, 23.8 mmol) was dissolved in aqueous methylamine (40 mL, 40 wt % in H2 O) at 10 C. under a nitrogen atmosphere. After 20 minutes, the reaction mixture was warmed to room temperature and stirred for 1 hour. The mixture was diluted with water and extracted with dichloromethane. The organic phase was dried (MgSO4) and concentrated to afford crude product which was purified by flash column chromatography (5% methanol/dichloromethane) to afford 3.18 g (82%) of pure product as a yellow oil. 1 H NMR (CDCl3): delta7.72 (m, 1H, ArH), 7.54 (m, 1H, ArH), 7.33 (m, 2H, ArH), 4.08 (s, 2H, CH2 NHCH3), 2.56 (CH2 NHCH3).
3.18 g (82%) In water; methylamine; Step 2) Preparation of 2-(Methylaminomethyl)benzoxazole 2-(Chloromethyl)benzoxazole (3.99 g, 23.8 mmol) was dissolved in aqueous methylamine (40 mL, 40 wt % in H2 O) at 10 C. under a nitrogen atmosphere. After 20 minutes, the reaction mixture was warmed to room temperature and stirred for 1 hour. The mixture was diluted with water and extracted with methylene chloride. The organic phase was dried (MgSO4) and concentrated to afford crude product which was purified by flash column chromatography (5% MeOH/CH2 Cl2) to afford 3.18 g (82%) of pure product as a yellow oil. 1 H NMR (CDCl3): delta7.72 (m, 1H, ArH), 7.54 (m, 1H, ArH), 7.33 (m, 2H, ArH), 4.08 (s, 2H, CH2 NHCH3), 2.56 (CH2 NHCH3).
 

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