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Chemical Structure| 1203605-31-5 Chemical Structure| 1203605-31-5

Structure of 1203605-31-5

Chemical Structure| 1203605-31-5

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Product Details of [ 1203605-31-5 ]

CAS No. :1203605-31-5
Formula : C12H15N3O2S
M.W : 265.33
SMILES Code : O=C(OC(C)(C)C)NCC(S1)=NC2=C1C=CN=C2
MDL No. :MFCD30535655

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Application In Synthesis of [ 1203605-31-5 ]

* 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 [ 1203605-31-5 ]

[ 1203605-31-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 89226-13-1 ]
  • [ 105752-11-2 ]
  • [ 1203605-31-5 ]
YieldReaction ConditionsOperation in experiment
83% With calcium oxide;tris(dibenzylideneacetone)dipalladium(0) chloroform complex; 1,1'-bis(diphenylphosphino)ferrocene; In acetonitrile; at 60℃;Inert atmosphere; A solution of 3-amino-4-iodopyridine (500 mg, 2.27 mmol), tris(dibenzylideneacetone)dipalladium(0) (63.6 mg, 0.07 mmol), dppf (155 mg, 0.28 mmol), calcium (II) oxide (255 mg, 4.55 mmol) and tert-butyl-2-amino-2-thioxoethylcarbamate (600 mg, 3.15 mmol) in anhydrous acetonitrile (4.5 mL) was degassed and stirred under argon atmosphere at 60C overnight. The solution was filtered over a pad of celite, rinsed with dichloromethane, methanol, ethyl acetate, and evaporated. Purification by flash chromatography (silica gel, dichloromethane/methanol 1/0 to 95/5) led to tert-butyl [1,3]thiazolo[4,5-c]pyridin-2-ylmethylcarbamate (500 mg, 83%) as a yellow oil. ESI-MS m/z 266 (M+H)+.
61.6% To a stirred solution of 4-iodopyridin-3-amine (500 mg, 2.2 mmol) in acetonitrile (5 mL) wasadded tert-butyl (2-amino-2-thioethoxyethyl)carbamate (561 mg, 2.9 mmol) and CaO (255 mg,4.5 mmol) at room temperature. The reaction mixture was purged with argon for 15 minutes,then dppf (151 mg, 0.27 mmol) and Pd2(dba)3 (64 mg, 0.06 mmol) was added to the reactionmixture. The reaction mixture was purged with argon for further 5 minutes and stirred in sealedtube at 60 C for 16 h. The reaction mixture was filtered through celite pad and washed the pad
 

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