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Chemical Structure| 1379982-43-0 Chemical Structure| 1379982-43-0

Structure of 1379982-43-0

Chemical Structure| 1379982-43-0

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Product Details of [ 1379982-43-0 ]

CAS No. :1379982-43-0
Formula : C11H11ClN4O2S
M.W : 298.75
SMILES Code : O=S(C1=CC(NC2=NC=CC(Cl)=N2)=CC=C1C)(N)=O

Safety of [ 1379982-43-0 ]

Application In Synthesis of [ 1379982-43-0 ]

* 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 [ 1379982-43-0 ]

[ 1379982-43-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3934-20-1 ]
  • [ 6973-09-7 ]
  • [ 1379982-43-0 ]
YieldReaction ConditionsOperation in experiment
With sodium hydrogencarbonate; In tetrahydrofuran; ethanol; at 70 - 75℃; for 13h; To a mixture of <strong>[6973-09-7]5-amino-2-methylbenzenesulfonamide</strong> (20 gm) in ethanol (208 ml) and tetrahydrofuran (52 ml) was added 2,4-dichloropryrimidine (44 gm) and sodium bicarbonate (36 gm) at room temperature. The contents were heated to 70 to 75°C and maintained for 13 hours. The reaction mass was then cooled to 10°C and maintained for 2 hours. The reaction mass was filtered and the solvent was distilled off under vacuum at below 50 to 55°C to obtain a residual mass. To the residual mass was added ethyl acetate (100 ml) and stirred for 1 hour, filtered. The solid obtained was dried to give 15.5 gm of 5-(4-chloropyrimidin-2ylamino)-2-methylbenzenesulfonamide.
15.5 g With sodium hydrogencarbonate; In tetrahydrofuran; ethanol; at 20 - 75℃; for 13h; To a mixture of <strong>[6973-09-7]5-amino-2-methylbenzenesulfonamide</strong> (20 gm) in ethanol (208 ml) and tetrahydrofuran (52 ml) was added 2,4-dichloropryrimidine (44 gm) and sodium bicarbonate (36 gm) at room temperature. The contents were heated to 70 to 75° C. and maintained for 13 hours. The reaction mass was then cooled to 10° C. and maintained for 2 hours. The reaction mass was filtered and the solvent was distilled off under vacuum at below 50 to 55° C. to obtain a residual mass. To the residual mass was added ethyl acetate (100 ml) and stirred for 1 hour, filtered. The solid obtained was dried to give 15.5 gm of 5-(4-chloropyrimidin-2ylamino)-2-methylbenzenesulfonamide
  • 2
  • [ 1376676-65-1 ]
  • [ 1379982-43-0 ]
  • pazopanib hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
5-(4-Chloropyrimidin-2ylamino)-2-methylbenzenesulfonamide (17 gm) as obtained in example 1, <strong>[1376676-65-1]N,2,3-trimethyl-2H-indazol-6-amine</strong> (10 gm) as obtained in example 2 and ethanol (166 ml) were added at room temperature and then heated to reflux. The reaction mass was maintained for 3 hours at reflux and then added concentrated hydrochloric acid (1 ml). The reaction mass was maintained for 10 hours at reflux and then cooled to room temperature. The separated solid was filtered and dried to obtain 17 gm of pazopanib hydrochloride (HPLC Purity: 97.5%).
17 g 5-(4-Chloropyrimidin-2ylamino)-2-methylbenzenesulfonamide (17 gm) as obtained in example 1, <strong>[1376676-65-1]N,2,3-trimethyl-2H-indazol-6-amine</strong> (10 gm) as obtained in example 2 and ethanol (166 ml) were added at room temperature and then heated to reflux. The reaction mass was maintained for 3 hours at reflux and then added concentrated hydrochloric acid (1 ml). The reaction mass was maintained for 10 hours at reflux and then cooled to room temperature. The separated solid was filtered and dried to obtain 17 gm of pazopanib hydrochloride (HPLC Purity: 97.5%).
 

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