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1H-Pyrazolo(3,4-d)pyrimidine → HCID 178506576, compound

HRID 570537
Notes
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Reaction equation

HRID 570537 reaction equation
[NH:1]1[C:5]2=[N:6][CH:7]=[N:8][CH:9]=[C:4]2[CH:3]=[N:2]1.[I:10]N1C(=O)CCC1=O>CN(C=O)C>[I:10][C:3]1[C:4]2[C:5](=[N:6][CH:7]=[N:8][CH:9]=2)[NH:1][N:2]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 674991H-Pyrazolo(3,4-d)pyrimidineHCID 120273N-Iodosuccinimide

Product 1

HCID 178506576HCID 178506576, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
80 °C

Procedure

520 mg (4.331 mmol) of 1H-pyrazolo[3,4-d]pyrimidine and 1.461 g (6.496 mmol) of N-iodosuccinimide were dissolved in 10 ml of DMF and the mixture was heated at 80° C. for 3 h. After cooling, the mixture was concentrated on a rotary evaporator and the residue was stirred with dichloromethane, filtered off with suction and dried under high vacuum. 569 mg (53% of theory) of the target compound were obtained.

Workup

  1. temperatureAfter cooling
  2. concentrationthe mixture was concentrated on a rotary evaporator
  3. filtrationfiltered off with suction
  4. customdried under high vacuum
  5. custom569 mg (53% of theory) of the target compound were obtained

Sources & evidence

ORD record
ord-a880a7ad8070471db5b646bbf75b8202
Source dataset
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09023849B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes