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Chemical Structure| 1398054-54-0 Chemical Structure| 1398054-54-0

Structure of 1398054-54-0

Chemical Structure| 1398054-54-0

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Product Details of [ 1398054-54-0 ]

CAS No. :1398054-54-0
Formula : C14H16ClNOS
M.W : 281.80
SMILES Code : COC1=C(SC(C)(C)C)C=C2C(Cl)=CC=NC2=C1
MDL No. :MFCD28962656

Safety of [ 1398054-54-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1398054-54-0 ]

* 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 [ 1398054-54-0 ]

[ 1398054-54-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1123-93-9 ]
  • [ 1398054-54-0 ]
  • N-1,3-benzothiazol-5-yl-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)quinolin-4-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
94% In isopropyl alcohol; at 150℃; for 0.25h;Irradiation; 4-chloro-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)quinoline (0.20 g, (0.66 mmol) and <strong>[1123-93-9]1,3-benzothiazol-5-amine</strong> (0.10 g, 0.66 mmol) were irradiated in microwave at 150° C. for 15 mins in isopropanol (2 mL). The reaction mixture was concentrated and purified via flash chromatography (0-50percent EtOAc/hexanes, 0-5percent MeOH/DCM). . N-1,3-benzothiazol-5-yl-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)quinolin-4-amine (0.26 g, 0.67 mmol, 94percent yield) was obtained.
94% In isopropyl alcohol; at 150℃; for 0.25h;Microwave irradiation; Step 1. N-1,3-benzothiazol-5-yl-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)-4-quinolinamine: 4-chloro-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)quinoline (0.20 g, 0.66 mmol) and <strong>[1123-93-9]1,3-benzothiazol-5-amine</strong> (0.10 g, 0.66 mmol) in isopropanol (2 mL) were irradiated by microwave at 150 °C for 15 mins. The reaction mixture was concentrated, purified via flash chromatography (0-50percent EtOAc/Hexane, 0-5percent MeOH/DCM) to yield N-1,3-benzothiazol-5-yl-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)-4-quinolinamine (0.26 g, 0.67 mmol, 94 percent yield). 1H NMR (400 MHz, DMSO-d) delta ppm 1.28 (s, 9H), 3.93 (s, 3H), 6.90 (d, J= 5.3 Hz, 1H), 7.32 (s, 1H), 7.54 (dd, J= 8.6 Hz, 2 Hz, 1H), 8.02 (d, J= 2 Hz, 1H), 8.18 (d, J= 8.6 Hz, 1H), 8.42 (d, J= 5.3 Hz, 1H), 8.60 (s, 1H), 9.27 (s, 1H), 9.42 (s, 1H). MS (m/z) 396 (M+H+).
94% In isopropyl alcohol; at 150℃; for 0.25h;Microwave irradiation; 4-Chloro-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)quinoline (0.20 g, 0.66 mmol) and 1,3-benzothiazole-5 -amine (0.10 g, 0.66 mmol) in isopropanol (2 mL) was irradiated with microwave at 15OC for 15 mins. The reaction mixture is concentrated,Purification via flash chromatography (0-50percent EtOAc/hexane,0-5percent MeOH/DCM),N-1,3-benzothiazol-5-yl-6-[(1,1-dimethylethyl)thio]-7-(methyloxy)-4-aminoquinoline is obtained(0.26 g, 0.67 mmol, 94percent yield).
 

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