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[ CAS No. 302964-08-5 ] {[proInfo.proName]}

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Chemical Structure| 302964-08-5
Chemical Structure| 302964-08-5
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Product Details of [ 302964-08-5 ]

CAS No. :302964-08-5 MDL No. :MFCD11045075
Formula : C16H13Cl2N5OS Boiling Point : -
Linear Structure Formula :- InChI Key :LMXUWARKUIELGT-UHFFFAOYSA-N
M.W : 394.28 Pubchem ID :11269410
Synonyms :

Safety of [ 302964-08-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 302964-08-5 ]

* 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 [ 302964-08-5 ]

[ 302964-08-5 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 103-76-4 ]
  • [ 302964-08-5 ]
  • [ 863127-77-9 ]
YieldReaction ConditionsOperation in experiment
83.2% To a mixture of compound 5D (4.00 g, 10.14 mmol) and hydroxyethylpiperazine (6.60 g, 50.69 mmol) in n-butanol (40 mL) was added DIPEA (3.53 mL, 20.26 mmol). The slurry was heated at 118°C for 4.5h, then cooled slowly to room temperature. The solid was collected by vacuum filtration, washed with n- butanol (5 mL), and dried. The product (5.11 g) was dissolved in hot 80percent EtOH-H2O (80 mL), and the solution was clarified by filtration. The hot solution was slowly diluted with water (15 mL) and cooled slowly to room temperature. The solid was collected by vacuum filtration, washed with 50percent ethanol-water (5 mL) and dried affording 4.27 g (83.2 percent yield) of N- (2-chloro-6-methylphenyl)-2- (6- (4- (3- hydroxyethyl) piperazin-1-yl)-2-methylpyrimidin-4-ylamino) thiazole-5-carboxamide as monohydrate. 1H NMR (400 MHz, DMSO-d6) # 2.23 (s, 3H), 2.40 (s, 3H), 2.42 (t, 2H, J=6), 2.48 (t, 4H, J=6.3), 3.50 (m, 4H), 3.53 (q, 2H, J=6), 4.45 (t, 1H, J=5.3), 6.04 (s, 1H), 7.25 (t, 1H, J=7.6), 7.27 (dd, 1H, J=7.6, 1.7), 7.40 (dd, 1H, J=7.6, 1.7), 8.21 (s, 1H), 9. 87 (s, 1H), 11.47.
Example 23; Procedure for the Preparation of Dasatinib Form H1-7 (Monohydrate)A mixture of compound 1 (133.9 mg, 0.5 mmol), N-(2-hydroxyethyl)piperazine (260.4 mg, 2 mmol) and N-ethyldiisopropylamine (0.174 ml, 1 mmol) in DMF (0.5 ml) was stirred at 100° C. for 2.5 h. H2O (3 ml) was added to the solution at the same temperature. A gummy product precipitated. The suspension was allowed to cool slowly to room temperature and stirred for 2 h at room temperature. The product was filtered washed with H2O (2.x.) and dried on the filter. Yield: 140 mg.
  • 2
  • [ 2632-65-7 ]
  • [ 302964-08-5 ]
  • [ 1587622-99-8 ]
  • 3
  • [ 29608-05-7 ]
  • [ 302964-08-5 ]
  • [ 1587623-06-0 ]
  • 4
  • [ 863127-76-8 ]
  • [ 302964-08-5 ]
  • 5
  • [ 1003-61-8 ]
  • [ 302964-08-5 ]
  • C20H16ClN7O2S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In 1,4-dioxane; Compound 32 can be synthesized as shown n Scheme 6.
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