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Water → HCID 178486780, compound

HRID 2404233
Notes
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Reaction equation

HRID 2404233 reaction equation
B(Br)(Br)Br.ClCCl.C([O:15][C:16]1[C:25]([O:26][CH3:27])=[CH:24][C:23]2[N:22]=[CH:21][C:20]3[N:28]([CH3:39])[N:29]=[C:30]([C:31]4[CH:38]=[CH:37][C:34]([C:35]#[N:36])=[CH:33][CH:32]=4)[C:19]=3[C:18]=2[CH:17]=1)C1C=CC=CC=1.O>FC(F)(F)C(O)=O>[OH:15][C:16]1[C:25]([O:26][CH3:27])=[CH:24][C:23]2[N:22]=[CH:21][C:20]3[N:28]([CH3:39])[N:29]=[C:30]([C:31]4[CH:38]=[CH:37][C:34]([C:35]#[N:36])=[CH:33][CH:32]=4)[C:19]=3[C:18]=2[CH:17]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 6344DichloromethaneHCID 25134Boron tribromideHCID 666321634-(8-benzyloxy-7-methoxy-3-methyl-3H-pyrazolo[3,4-c]quinolin-1-yl)benzonitrile

Product 1

HCID 178486780HCID 178486780, compoundYield 95.3%

Reagents, catalysts & solvents 1

HCID 6422
Trifluoroacetic acid
Solvent

Procedure

A 1.0 M boron tribromide solution in dichloromethane (38.2 ml, 38.2 mmol) is slowly added dropwise to a solution of 4-(8-benzyloxy-7-methoxy-3-methyl-3H-pyrazolo[3,4-c]quinolin-1-yl)benzonitrile (3.82 g, 9.09 mmol) in trifluoroacetic acid (38 ml) under a dry nitrogen atmosphere with ice-bath cooling. When the addition is complete, the mixture is subsequently stirred for a further 30 min. When the reaction is complete (HPLC-MS check), the reaction mixture is carefully added to water (800 ml) and extracted twice with ethyl acetate (200 ml each time). The combined organic phases are washed with water (150 ml) and semi-saturated NaHCO3 solution (200 ml), subsequently dried using Na2SO4 and filtered with suction. The filtrate is evaporated in vacuo, suspended in a little ethanol, filtered off with suction and dried in a high vacuum, giving the title compound 4-(8-hydroxy-7-methoxy-3-methyl-3H-pyrazolo[3,4-c]quinolin-1-yl)benzonitrile (2.86 g, 8.66 mmol) as a solid having a melting point of 288.9° C. MS: 331.1 (M+H+), TLC (HPTLC): Rf=0.34 (ethyl acetate/ethanol 8:1, parts by volume).

Workup

  1. temperaturecooling
  2. additionWhen the addition
  3. extractionextracted twice with ethyl acetate (200 ml each time)
  4. washThe combined organic phases are washed with water (150 ml) and semi-saturated NaHCO3 solution (200 ml)
  5. customsubsequently dried
  6. filtrationfiltered with suction
  7. customThe filtrate is evaporated in vacuo
  8. filtrationfiltered off with suction
  9. customdried in a high vacuum

Sources & evidence

ORD record
ord-20c95830fe3846cfb2411c5e4d313900
Source dataset
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08802712B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes