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Chemical Structure| 139272-29-0 Chemical Structure| 139272-29-0

Structure of 139272-29-0

Chemical Structure| 139272-29-0

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Product Details of [ 139272-29-0 ]

CAS No. :139272-29-0
Formula : C8H13N3O2S
M.W : 215.27
SMILES Code : O=S(CC1=CC=C(NN)C=C1)(NC)=O
MDL No. :MFCD00671706

Safety of [ 139272-29-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H317-H320
Precautionary Statements:P261-P264-P270-P272-P280-P301+P310+P330-P302+P352-P305+P351+P338-P333+P313-P337+P313-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 139272-29-0 ]

* 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 [ 139272-29-0 ]

[ 139272-29-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 109903-35-7 ]
  • [ 139272-29-0 ]
YieldReaction ConditionsOperation in experiment
Intermediate A24: 1 -(4-(5-Amino-3-ferf-butyl-1 H-pyrazol-1 -yl)phenyl)-/V-methyl methanesulfonamide.Intermediate A24To a suspension of 1-(4-aminophenyl)-A/-methylmethanesulfonamide (500 mg, 2.50 mmol) in hydrochloric acid (6 M, 10 mL) at 0C was added a soution of sodium nitrite (181 mg, 2.62 mmol) in water (3.0 mL) over 5 min. The reaction mixture was maintained at 0C for 2.5 hr, was treated with tin(ll) chloride (1.33 g, 6.99 mmol) in hydrochloric acid (6M, 15 mL) and was then warmed to RT for 64 hr. The resulting mixture was basified to pH 12 with aq NaOH (6.0 M) and was extracted with EtOAc (2 x 100 mL). The combined organic extracts were washed with water and then dried and evaporated in vacuo to give a residue that was suspended in ethanol (10 mL) and treated with 4,4-dimethyl-3-oxopentanenitrile (160 mg, 1.3 mmol) and cone hydrochloric acid (12 M, 106 mu, 1.27 mmol). The resulting mixture was heated at reflux for 5 hr and after a further 23 hr at RT was evaporated in vacuo, to remove the ethanol and the resulting aq mixture basified with aq NaOH (2.0 M) and then extracted with DCM (2 x 30 mL). The combined organic extracts were dried and evaporated in vacuo to afford the title compound, Intermediate A24, as an orange solid (146 mg, 85% purity, 15%); R1 1 .34 min (Method 2); m/z 323 (M+H)+, (ES+). This material was used in subsequent steps without further purification
Intermediate A13: 1 -(4-(5-Amino-3-ieri-butyl-1 H-pyrazol-1 -yl)phenyl)-yV-methyl methanesulfonamide.; Intermediate A13; To a suspension of 1 -(4-aminophenyl)-/V-methylmethanesulfonamide (500 mg, 2.50 mmol) in hydrochloric acid (6 M, 10 mL) at 0C was added a soution of sodium nitrite (181 mg, 2.62 mmol) in water (3.0 mL) over 5 min. The reaction mixture was maintained at 0C for 2.5 hr, was treated with tin(ll) chloride (1.33 g, 6.99 mmol) in hydrochloric acid (6M, 15 mL) and was then warmed to RT for 64 hr. The resulting mixture was basified to pH 12 with aq NaOH (6.0 M) and was extracted with EtOAc (2 x 100 mL). The combined organic extracts were washed with water and then dried and evaporated in vacuo to give a residue that was suspended in ethanol (10 mL) and treated with 4,4-dimethyl-3-oxopentanenitrile (160 mg, 1 .3 mmol) and cone hydrochloric acid (12 M, 106 mu, 1 .27 mmol). The resulting mixture was heated at reflux for 5 hr and after a further 23 hr at RT was evaporated in vacuo, to remove the ethanol. The resulting aq mixture was basified with aq NaOH (2.0 M) and was then extracted with DCM (2 x 30 mL). The combined organic extracts were dried and evaporated in vacuo to afford the title compound, Intermediate A13, as an orange solid (146 mg, 85% purity, 15%); R' 1.34 min (Method 2); m/z 323 (M+H)+, (ES+). This material was used in subsequent steps without further purification.
Intermediate A13: 1-(4-(5-Amino-3-tert-butyl-1H-pyrazol-1-yl)phenyl)-N-methyl methanesulfonamide To a suspension of <strong>[109903-35-7]1-(4-aminophenyl)-N-methylmethanesulfonamide</strong> (500 mg, 2.50 mmol) in hydrochloric acid (6 M, 10 mL) at 0 C. was added a solution of sodium nitrite (181 mg, 2.62 mmol) in water (3.0 mL) over 5 min. The reaction mixture was maintained at 0 C. for 2.5 hr, was treated with tin(II) chloride (1.33 g, 6.99 mmol) in hydrochloric acid (6M, 15 mL) and was then warmed to RT for 64 hr. The resulting mixture was basified to pH 12 with aq NaOH (6.0 M) and was extracted with EtOAc (2*100 mL). The combined organic extracts were washed with water and then dried and evaporated in vacuo to give a residue that was suspended in ethanol (10 mL) and treated with 4,4-dimethyl-3-oxopentanenitrile (160 mg, 1.3 mmol) and conc hydrochloric acid (12 M, 106 muL, 1.27 mmol). The resulting mixture was heated at reflux for 5 hr and after a further 23 hr at RT was evaporated in vacuo, to remove the ethanol. The resulting aq mixture was basified with aq NaOH (2.0 M) and was then extracted with DCM (2*30 mL). The combined organic extracts were dried and evaporated in vacuo to afford the title compound, Intermediate A13, as an orange solid (146 mg, 85% purity, 15%); Rt 1.34 min (Method 2); m/z 323 (M+H)+, (ES+). This material was used in subsequent steps without further purification.
 

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