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[ CAS No. 1027643-30-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1027643-30-6
Chemical Structure| 1027643-30-6
Structure of 1027643-30-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1027643-30-6 ]

CAS No. :1027643-30-6 MDL No. :MFCD04966888
Formula : C11H13ClN2S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 240.75 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1027643-30-6 ]

* 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 [ 1027643-30-6 ]

[ 1027643-30-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1203605-21-3 ]
  • [ 1027643-30-6 ]
  • [ 1203604-53-8 ]
YieldReaction ConditionsOperation in experiment
98% With N-ethyl-N,N-diisopropylamine In acetonitrile at 85℃; Inert atmosphere; 62 Under argon, a solution of 3-chloro-5-(2,6-dimethoxyphenyl)-1,2,4-triazine (16.4 mg, 0.065 mmol, prepared as in example 41), 2-pyrrolidin-2-yl-1,3-benzothiazole hydrochloride (23.5 mg, 0.098 mmol) and DIPEA (28 µL, 0.16 mmol) in anhydrous acetonitrile (0.25 mL) was stirred at 85°C overnight. The solution was then concentrated and the residue was purified by preparative TLC (silica gel, dichloromethane/methanol 95/5) to afford 2-{1-[5-(2,6-dimethoxyphenyl)-1,2,4-triazin-3-yl]pyrrolidin-2-yl}-1,3-benzothiazole (26.8 mg, 98%) as a pale yellow oil. ESI-MS m/z 420 (M+H)+. 1H NMR (CDCl3), δ (ppm): 8.58 (s, 1H), 7.95 (d, J = 8.0 Hz, 1H), 7.80 (d, J = 8.0 Hz, 1H), 7.43 (t, J= 7.9 Hz, 1H), 7.32 (t, J = 8.0 Hz, 2H), 6.53 (d, J = 7.9 Hz, 2H), 5.75 (br s, 1H), 4.15 (br s, 1H), 3.89 (br s, 1H), 3.45 (br s, 6H), 2.54-2.41 (m, 2H), 2.30-2.01 (m, 2H).
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