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Chemical Structure| 507487-90-3 Chemical Structure| 507487-90-3

Structure of 507487-90-3

Chemical Structure| 507487-90-3

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Product Details of [ 507487-90-3 ]

CAS No. :507487-90-3
Formula : C12H18N4OS
M.W : 266.36
SMILES Code : CN(C)/C=N/C1=NC(C)=C(C(/C=C/N(C)C)=O)S1
MDL No. :MFCD28977334

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Application In Synthesis of [ 507487-90-3 ]

* 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 [ 507487-90-3 ]

[ 507487-90-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 30748-47-1 ]
  • [ 4637-24-5 ]
  • [ 507487-90-3 ]
YieldReaction ConditionsOperation in experiment
at 100℃; for 15h; A mixture of <strong>[30748-47-1]5-acetyl-2-amino-4-methylthiazole</strong> (12.5 g) and N,N-dimethylformamide-dimethylacetal (35.4 ml) is heated for 15 hours at 100 C. After cooling to room temperature the reaction mixture is evaporated, triturated with ethyl acetate, and filtered to give the title compound as an orange solid. MS (Method D) M+H 267.
  • 2
  • [ 30748-47-1 ]
  • [ 4637-24-5 ]
  • [ 507487-90-3 ]
YieldReaction ConditionsOperation in experiment
82% at 20 - 103℃; for 21h; 5-Acetyl-2-amino-4-methylthiazole(30 g, 192 mmol) was added portion wise to N,N-dimethylformamide dimethyl acetal (90ml, ex Aldrich), over 1 hour, at room temperature. The resulting pale-yellowsuspension was then heated at reflux for 20 hours, cooled to room temperatureand EtOAc (150 ml) added. After stirring the suspension for 30 minutes at roomtemperature the first crop of crystals of compound 7 were collected by filtration, washing with EtOAc (2x 50 ml). Thefiltrate was evaporated and the residue suspended in EtOAc (50 ml), triturated,stirred, and then filtered to give a second crop of crystals. The two cropswere combined and dried under high vacuum to give compound 7 as an orange crystalline solid, 44.4 g (95% purity, 82% yield).mp: 157-159 C. 1H NMRin CDCl3 (400 MHz): 8.23 (s, 1H), 7.68 (d, J = 12.1 Hz, 1H), 5.35 (d, J= 12.1 Hz, 1H), 3.11 (s, 3H), 3.08 (s, 3H), 2.63 (s, 3H), 1.56 (s, 6H).
at 100℃; Step 42.2: 4-Methyl-5-[2-(1 -methyl-cvclopropyD-pyrimidin^-yli-thiazol^-ylamine; Powdered sodium hydroxide (5.86 g) is added to a solution of N'-[5-(3-dimethylamino- acryloyl)-4-methyl-thiazol-2-yl]-N,N-dimethyl-formamidine (13 g, prepared as described byS. Wang et al J. Med. Chem. 2004, 47, 1662-1675.) and 1-methyl- cyclopropanecarboxamidine hydrochloride (7.2 g, prepared as described in EP0227415) in2-methoxyethanol (98 ml) and the mixture heated at 125 0C for 1 hour with stirring. The reaction mixture is cooled, water is added, and the title compound isolated by filtration. ESI- MS: M+H 247 and M-H 245.
 

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