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Chemical Structure| 1422827-96-0 Chemical Structure| 1422827-96-0

Structure of 1422827-96-0

Chemical Structure| 1422827-96-0

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Product Details of [ 1422827-96-0 ]

CAS No. :1422827-96-0
Formula : C14H19IN6O2
M.W : 430.24
SMILES Code : O=C(N1C[C@H](N2N=C(I)C3=C(N)N=CN=C32)CC1)OC(C)(C)C
MDL No. :MFCD31628847

Safety of [ 1422827-96-0 ]

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 [ 1422827-96-0 ]

* 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 [ 1422827-96-0 ]

[ 1422827-96-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 109431-87-0 ]
  • [ 151266-23-8 ]
  • [ 1422827-96-0 ]
YieldReaction ConditionsOperation in experiment
84% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20℃; A solution of 4-amino-3-iodo-lH-pyrazolo [3,4-D] pyrimidine (10 g, 38 mmol)(R) -1-Boc-3-hydroxypyrrole (16 g, 85 mmol)Triphenylphosphine (20 g, 76 mmol) was added to a three-necked flask,THF (120 ml) was added,Cooling to 0 ,A mixture of diisopropyl azodicarboxylate (DIAD) (15.2 g, 76 mmol) and THF (30 ml)About 1h drops finished,Slowly warmed to room temperature overnight.The reaction solution was spin-dried,Extracted with water, extracted with ethyl acetate, dried and concentrated to give the product (13.8 g, yield 84%) by column chromatography.
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20℃; for 12h; General procedure: Toa stirred solution of 3-Iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine 10 (10 mmol) and triphenylphosphine (20 mmol) in THF (25 mL) wasadded 11a-11e (20 mmol) and DIAD (20mmol) at 0,it was stirred at room temperature for 12h. Then the mixture was concentratedto a residue and purified via column chromatography (0% ethyl acetate indichloromethane to 80%) to provide the desired compound 12a-12e (Yield: 39%-55%).
 

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