Hydrochloric Acid → HCID 69516122, compound

HRID 1351100Notes

Reaction equation

HRID 1351100 reaction equation
[CH3:1][C:2]1[CH:48]=[CH:47][C:46]([CH3:49])=[CH:45][C:3]=1[CH2:4][O:5][C:6]1[CH:44]=[CH:43][CH:42]=[CH:41][C:7]=1[CH2:8][C:9]1[C:10]([O:17][C@@H:18]2[O:35][C@H:34]([CH2:36][O:37]C(=O)C)[C@@H:29]([O:30]C(=O)C)[C@H:24]([O:25]C(=O)C)[C@H:19]2[O:20]C(=O)C)=[N:11][NH:12][C:13]=1[CH:14]([CH3:16])[CH3:15].C[O-].[Na+].Cl>O1CCCC1.CO>[CH3:1][C:2]1[CH:48]=[CH:47][C:46]([CH3:49])=[CH:45][C:3]=1[CH2:4][O:5][C:6]1[CH:44]=[CH:43][CH:42]=[CH:41][C:7]=1[CH2:8][C:9]1[C:10]([O:17][C@@H:18]2[O:35][C@H:34]([CH2:36][OH:37])[C@@H:29]([OH:30])[C@H:24]([OH:25])[C@H:19]2[OH:20])=[N:11][NH:12][C:13]=1[CH:14]([CH3:16])[CH3:15]

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 10942334Sodium MethoxideHCID 69517514HCID 69517514, compound

Product 1

HCID 69516122HCID 69516122, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 8028TetrahydrofuranSolvent

Procedure

To a solution of 4-[2-(2,5-dimethylbenzyloxy)benzyl]-5-isopropyl-1,2-dihydropyrazol-3-one (152 mg) in N,N-dimethylformamide (1 mL) was added sodium hydride (60%, 18 mg), and the mixture was stirred at room temperature for 15 minutes. To the reaction mixture was added a solution of acetobromo-α-D-glucose (214 mg) in N,N-dimethylformamide (1 mL), and the resulting mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on aminopropyl silica gel (eluent: ethyl acetate/hexane=1/1-ethyl acetate) to give 4-[2-(2,5-dimethylbenzyloxy)benzyl]-5-isopropyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole. To a solution of 4-[2-(2,5-dimethylbenzyloxy)benzyl]-5-isopropyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole in tetrahydrofuran (1 mL) and methanol (0.5 mL) was added sodium methoxide (28% methanol solution, 0.400 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was neutralized with 2 mol/L hydrochloric acid and concentrated under reduced pressure, and the residue was purified by chromatography on silica gel (eluent: dichloromethane/methanol=10/1–5/1) to give the title compound (33 mg).

Workup

  1. concentrationconcentrated under reduced pressure
  2. customthe residue was purified by chromatography on silica gel (eluent: dichloromethane/methanol=10/1–5/1)

Sources & evidence

ORD record
ord-8638cfa29d4f49cc983fe26f41e57946
Source dataset
uspto-grants-2007_05
Patent number
US07217697B2

Reaction notes

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