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Chemical Structure| 872059-27-3 Chemical Structure| 872059-27-3

Structure of 872059-27-3

Chemical Structure| 872059-27-3

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Product Details of [ 872059-27-3 ]

CAS No. :872059-27-3
Formula : C7H6ClN3S
M.W : 199.66
SMILES Code : CSC1=NC(Cl)=CC2=NC=CN12
MDL No. :MFCD09033874

Safety of [ 872059-27-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 872059-27-3 ]

* 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 [ 872059-27-3 ]

[ 872059-27-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 107-20-0 ]
  • [ 1005-38-5 ]
  • [ 872059-27-3 ]
YieldReaction ConditionsOperation in experiment
60% In N,N-dimethyl-formamide; at 100℃; Referring to Scheme 1, 4-amino-6-chloro-2-(methylthio)-pyrimidine (1.0 g, 5.7 mmol) and chloroacetaldehyde (2 ml, 14.2 mmol) were mixed in DMF (5 ml). The solution was stirred overnight at 100° C. DMF was removed in vacuo and the residue was purified by flash chromatography with 1:10 MeOH:DCM to leave 7-chloro-5-(methylthio)imidazo[1,2-f]pyrimidine as a brown solid (68 mg, 60percent). 1H NMR (400 MHz, CD3OD) delta 7.93 (s, 1H) 7.74 (d, J=1.5 Hz, 1H) 7.62 (s, 1H) 3.27 (s, 3H). [M+H] calc'd for C7H6ClN3S, 200; found, 200.
In ethanol; for 2.5h;Heating / reflux; A mixture of 6-chloro-2-methylsulfanyl-pyrimidin-4-ylamine (0.9 g, 5.14 mmol) and chloroacetaldehyde (6.5 mL, 51.4 mmol) in ethanol (10 mL) was heated to reflux for 2.5 h and brought to RT. The mixture was concentrated and the residue obtained was dissolved in dichloromethane, washed with saturated NaHCO3, brine, dried, concentrated and purified by column chromatography chromatography on silica gel using 0-4percent MeOH/CH2Cl2 to give as a white solid. MS m/z 200 (MH)+.
  • 2
  • [ 7252-83-7 ]
  • [ 1005-38-5 ]
  • [ 872059-27-3 ]
YieldReaction ConditionsOperation in experiment
66% In 1,4-dioxane; water; for 24h;Reflux; Example 9A; 7-Chloro-5-(methylthio)imidazo[1,2-c]pyrimidine 75 g (427 mmol) of 4-amino-6-chloro-2-(methylthio)pyrimidine are dissolved in 3000 ml of dioxane and 750 ml of water. 101.05 g (597.81 mmol) of bromoacetaldehyde dimethyl acetal are added, and the mixture is heated under reflux for 24 h. After the reaction is complete, the dioxane is removed in vacuo and the aqueous suspension is suspended in THF, filtered with suction and washed with some THF. Drying of the solid at 40° C. under high vacuum results in 56.5 g (66percent of theory) of the product.MS (ES+): m/z=200 (M+H)+.1H-NMR (400 MHz, DMSO-d6): delta=8.12 (s, 1H), 7.97 (s, 1H), 7.77 (s, 1H), 2.80 (s, 3H).
 

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