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Chemical Structure| 870997-57-2 Chemical Structure| 870997-57-2

Structure of 870997-57-2

Chemical Structure| 870997-57-2

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Product Details of [ 870997-57-2 ]

CAS No. :870997-57-2
Formula : C9H12N2O
M.W : 164.20
SMILES Code : O=C(NC)C1=CC=CC(C)=C1N
MDL No. :MFCD09042975
InChI Key :FBOWFVWOCBTBPH-UHFFFAOYSA-N
Pubchem ID :16770689

Safety of [ 870997-57-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P280

Application In Synthesis of [ 870997-57-2 ]

* 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 [ 870997-57-2 ]

[ 870997-57-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 66176-17-8 ]
  • [ 74-89-5 ]
  • [ 870997-57-2 ]
YieldReaction ConditionsOperation in experiment
92% With acetic acid; In water; ethyl acetate; at 35 - 37℃; for 3.33333h; EXAMPLE 5 u Preparation of 2-amino-5-chloro-N,3-dimethylbenzamide Step A: Preparation of 2-amino-N,3-dimethylbenzamideA mixture of 8-methyl-2No.-3,l-benzoxazine-2,4(lH)-dione (PCT Patent PublicationWO 00/27831) (18 g, 0.1 mol) and acetic acid (1.2 g, 0.02 mol) in ethyl acetate (200 mL) was warmed to 35 C, and aqueous methylamine (40%, 9.0 g, 0.12 mol) was added dropwise over 50 minutes at 35-37 0C. Then more aqueous methylamine (40%, 0.9 g, 12 mmol) was added, and the mixture was stirred an additional 2.5 h at 36 C. Then water (20 mL) was added, the layers were separated, and the organic layer was washed with water, dried(MgSC^), and evaporated to afford the title compound, 15.45 g (92%).1H NMR (CDCl3) delta 2.14 (s, 3H), 2.94 (d, 3H, J = 5 Hz), 5.37 (br s, 2H), 6.21 (br s, IH),6.56 (t, J = 7.5 Hz, IH), 7.10 (dd, J = 7.5 Hz, 7.5 Hz, IH), 7.18 (dd, J = 7.5 Hz, 7.5 Hz, IH).
47% In tetrahydrofuran; at 0 - 20℃; General procedure: A solution of 8-fluoro-1H-benzo[d][1,3]oxazine-2,4-dione (10.0 g, 55.4 mmol) in THF (100 mL) was chilled to 0 C and treated with a solution of methylamine in THF (2.0 M, 45 mL). The mixture was warmed to room temperature and stirred for 1.5 hours. The reaction was concentrated and the residue was triturated with ether (4 x 20 mL), and dried en vacuo. mp 94-97 C; LCMS: m/z = 169 (M+H+); 1H NMR (400 MHz, CDCl3) delta 8.30 (s, 1H), 7.32 (d, 1H, J = 8.0 Hz), 7.12 (m, 1H), 6.32 (br s, 2H), 6.07 (br s, 1H), 2.73 (d, 3H, J = 4.5 Hz).
 

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