Hydrochloric Acid → HCID 68952351, compound

HRID 1453883Notes

Reaction equation

HRID 1453883 reaction equation
[OH:1][C:2]1[C:3]([C:19]([O:21]CC)=[O:20])=[N:4][N:5]2[C@@H:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH2:9][N:8]([CH3:17])[C:7](=[O:18])[C:6]=12.[OH-].[Na+].Cl>CO>[OH:1][C:2]1[C:3]([C:19]([OH:21])=[O:20])=[N:4][N:5]2[C@@H:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH2:9][N:8]([CH3:17])[C:7](=[O:18])[C:6]=12

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 86617825HCID 86617825, compound

Product 1

HCID 68952351HCID 68952351, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
50 °C

Procedure

To a solution of ethyl (7S)-3-hydroxy-5-methyl-4-oxo-7-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate (0.30 g, 1.00 mmol) in MeOH (10 mL) was added aqueous 1N NaOH (5.97 mL, 5.97 mmol). The reaction was stirred at 50° C. overnight and quenched by the addition of aqueous 3N HCl (2.00 mL, 2.00 mmol). Purification by reverse phase chromatography on a C-18 column using a gradient elution of 95-5% H2O (0.1% TFA)/CH3CN (0.1% TFA) and collection and concentration of the appropriate fractions afforded the title product as a light pink solid. 1H NMR (400 MHz, d6-DMSO) δ 8.90 (bs, 1H), 7.37 (m, 3H), 7.08 (m, 2H), 5.74 (t, J=4.6 Hz, 1H), 4.15 (dd, J=13.4, 4.6 Hz, 1H), 3.86 (dd, J=13.4, 4.7 Hz, 1H), 2.89 (s, 3H); ES MS (M+1)=288.

Workup

  1. customPurification by reverse phase chromatography on a C-18 column
  2. washa gradient elution of 95-5% H2O (0.1% TFA)/CH3CN (0.1% TFA) and collection and concentration of the appropriate fractions

Sources & evidence

ORD record
ord-1a87190095c644879b49941624656b45
Source dataset
uspto-grants-2009_01
Patent number
US07476666B2

Reaction notes

Loading…