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Dimethylformamide → 2-chloro-5-(5-methyl-1H-pyrazol-3-yl)-benzoic acid methyl ester

HRID 1988371
Notes
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Reaction equation

HRID 1988371 reaction equation
[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[C:8]([C:10](=O)[CH3:11])[CH:7]=[CH:6][C:5]=1[Cl:13].CO[C:17](OC)([N:19](C)C)[CH3:18].C[N:25](C)C=O>CN(C)C(=O)C>[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[C:8]([C:10]2[CH:11]=[C:17]([CH3:18])[NH:19][N:25]=2)[CH:7]=[CH:6][C:5]=1[Cl:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6228DimethylformamideHCID 878351,1-Dimethoxyethyl(dimethyl)amineHCID 58818179Methyl 5-acetyl-2-chlorobenzoate

Product 1

HCID 588181962-chloro-5-(5-methyl-1H-pyrazol-3-yl)-benzoic acid methyl ester

Reagents, catalysts & solvents 1

HCID 31374DimethylacetamideSolvent

Procedure

A solution of 5-acetyl-2-chloro-benzoic acid methyl ester (1.58 g, 7.5 mmol) and N,N-dimethylacetamide dimethylacetal in N,N-dimethylformamide and N,N-dimethylacetamide was stirred at 90° C. for 3 h. The mixture was cooled to room temperature and concentrated in vacuo. The residue was diluted with ethanol (18 mL) and tetrahydrofuran (2 mL). Hydrazine hydrate (0.34 mL) was added and the mixture was stirred at room temperature for 16 h. The mixture was concentrated in vacuo. The residue was purified by flash column chromatography (gradient 0-10% methanol-ethyl acetate) to afford the title compound (1.0 g).

Workup

  1. concentrationconcentrated in vacuo
  2. additionThe residue was diluted with ethanol (18 mL) and tetrahydrofuran (2 mL)
  3. additionHydrazine hydrate (0.34 mL) was added
  4. concentrationThe mixture was concentrated in vacuo
  5. customThe residue was purified by flash column chromatography (gradient 0-10% methanol-ethyl acetate)

Sources & evidence

ORD record
ord-b3b383b9515748fead96a2b84a27ac18
Source dataset
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07553972B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes