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Chemical Structure| 869854-12-6 Chemical Structure| 869854-12-6

Structure of 869854-12-6

Chemical Structure| 869854-12-6

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Product Details of [ 869854-12-6 ]

CAS No. :869854-12-6
Formula : C6H7BrN2S
M.W : 219.10
SMILES Code : NC1=NC(C2CC2)=C(Br)S1
MDL No. :MFCD13193636

Safety of [ 869854-12-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P301+P310
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 869854-12-6 ]

* 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 [ 869854-12-6 ]

[ 869854-12-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 324579-90-0 ]
  • [ 869854-12-6 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; acetic acid; In acetonitrile; at 0℃; for 1h; To a solution of 4- cyclopropylthiazol-2-amine (5 g, 35.7 mmol, 1.0 equiv), 6.1 mL AcOH (106.8 mmol, 3 equiv) and 100 mL acetonitrile was added 6.35 g N-bromosuccinimide (35.7 mmol, 1.0 equiv) at 0 C. After stirring for 1 h, the suspension was diluted with saturated NaHC03 and extracted with EtOAc. The organics were washed with brine, dried with Na2S04 and concentrated under reduced pressure. Purification of the residue by flash chromatography (Si02, 20% EtOAc/Hexane) gave 4.12 g of the product as a brown solid (18.8 mmol).
With N-Bromosuccinimide; In 1-methyl-pyrrolidin-2-one; at 20℃; for 3h;Cooling with ice; General procedure: To a mixture of 8 (10.0g, 57mmol) and NMP (100mL) was added NBS (10.6g, 60mmol, 1.1equiv.) portionwise on ice water bath, and the whole was stirred on the same bath for 1hr, then at rt for 2hr. To the reaction mixture was added N-methylpiperazine (28.5g, 285mmol, 5.0equiv.) in NMP (20mL) on an ice water bath, and the whole was stirred at 100C for 8hr. To the reaction mixture was added H2O, and the whole was stirred at room temperature for 10min. The precipitate was collected by filtration, washed with H2O and dried in vacuo to give the title compound (12.5g, 45mmol, 80%) as a pale brown powder. 1H NMR (400MHz, CDCl3): delta=2.35 (3H, s), 2.50-2.63 (4H, m), 2.85-2.97 (4H, m), 4.80 (2H, s), 7.21-7.28 (1H, m, overlapped with CHCl3), 7.32-7.42 (2H, m), 8.04-8.14 (2H, m); MS (ESI) m/z 275 [M+H]+.
 

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