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Oxalic Acid → N-[4-(1,3-benzodioxol-5-yl)-1-(2-hydroxyethyl)-5-methoxy-1H-pyrazol-3-yl]-2-phenyl-1-ethanesulfonamide

HRID 1062767
Notes
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Reaction equation

HRID 1062767 reaction equation
C([O:4][CH2:5][CH2:6][N:7]1[C:11]([O:12][CH3:13])=[C:10]([C:14]2[CH:22]=[CH:21][C:17]3[O:18][CH2:19][O:20][C:16]=3[CH:15]=2)[C:9]([N:23](COC)[S:24]([CH2:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)(=[O:26])=[O:25])=[N:8]1)(=O)C.C(O)(=O)C(O)=O>O.CO>[O:18]1[C:17]2[CH:21]=[CH:22][C:14]([C:10]3[C:9]([NH:23][S:24]([CH2:27][CH2:28][C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)(=[O:26])=[O:25])=[N:8][N:7]([CH2:6][CH2:5][OH:4])[C:11]=3[O:12][CH3:13])=[CH:15][C:16]=2[O:20][CH2:19]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 971Oxalic AcidHCID 222819772-{4-(1,3-benzodioxol-5-yl)-5-methoxy-3-[(methoxymethyl)(phenethylsulfonyl)amino]-1H-pyrazol-1-yl}ethyl Acetate

Product 1

HCID 22281887N-[4-(1,3-benzodioxol-5-yl)-1-(2-hydroxyethyl)-5-methoxy-1H-pyrazol-3-yl]-2-phenyl-1-ethanesulfonamideYield 54.5%

Reagents, catalysts & solvents 2

HCID 887MethanolSolvent
HCID 962
Water
Solvent
2×

Procedure

2-{4-(1,3-Benzodioxol-5-yl)-5-methoxy-3-[(methoxymethyl)(phenethylsulfonyl)amino]-1H-pyrazol-1-yl}ethyl acetate (Preparation 54) (70 mg), oxalic acid (200 mg) were dissolved in a mixture of water (2 ml) and methanol (2 ml) and refluxed for two days. The reaction was diluted with water (10 ml) and the mixture was then extracted with dichloromethane (3×8 ml). The combined organic fractions were dried over sodium sulfate, concentrated under reduced pressure to yield a pale yellow oil which was purified by column chromatography (Sep-Pak™, 10 g) eluted with dichloromethane:methanol (97:3) to yield the title compound as a colourless oil (32 mg).

Workup

  1. temperaturerefluxed for two days
  2. extractionthe mixture was then extracted with dichloromethane (3×8 ml)
  3. dry with materialThe combined organic fractions were dried over sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customto yield a pale yellow oil which
  6. customwas purified by column chromatography (Sep-Pak™, 10 g)
  7. washeluted with dichloromethane:methanol (97:3)

Sources & evidence

ORD record
ord-f5f4abe5446748be9e26b8eb76420957
Source dataset
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06962923B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes