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Potassium Carbonate → HCID 135759101, compound

HRID 1719686
Notes
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Reaction equation

HRID 1719686 reaction equation
Cl.N[C:3]1[C:4]2[C:5](=[N:15][N:16]([CH3:18])[CH:17]=2)[NH:6][C:7]2[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][C:8]=2[N:9]=1.C(=O)([O-])[O-:20].[K+].[K+]>C(O)C.O>[Cl:14][C:11]1[CH:12]=[CH:13][C:7]2[NH:6][C:5]3=[N:15][N:16]([CH3:18])[CH:17]=[C:4]3[C:3](=[O:20])[NH:9][C:8]=2[CH:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 11430Potassium CarbonateHCID 135759094HCID 135759094, compound

Product 1

HCID 135759101HCID 135759101, compound

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent2×

Procedure

4-Amino-7-chloro-2,10-dihydro-2-methylpyrazolo[3,4-b][1,5]benzodiazepine hydrochloride (11.3 g) and potassium carbonate (16.8 g) were heated under reflux in a mixture of ethanol (200 ml) and water (20 ml) for 48 hours. Water (300 ml) was added and the solution cooled. The precipitate was crystallised from acetic acid to give the title compound m.p.>260° C.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperaturethe solution cooled
  2. customThe precipitate was crystallised from acetic acid

Sources & evidence

ORD record
ord-a1c9faef27364deb9a04b610f5e90160
Source dataset
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04542131

Reaction notes

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