Hydrochloric Acid → N-(2-hydroxyethyl)-N-{[1-(4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1H-pyrazol-4-yl]carbonyl}glycine

HRID 215786Notes

Reaction equation

HRID 215786 reaction equation
[OH:1][CH2:2][CH2:3][N:4]([C:13]([C:15]1[CH:16]=[N:17][N:18]([C:20]2[CH:25]=[CH:24][C:23]([O:26][CH2:27][CH2:28][CH2:29][N:30]3[CH2:34][CH2:33][CH2:32][C@H:31]3[CH3:35])=[CH:22][CH:21]=2)[CH:19]=1)=[O:14])[CH2:5][C:6]([O:8]C(C)(C)C)=[O:7].Cl>O1CCOCC1.C(OCC)(=O)C>[OH:1][CH2:2][CH2:3][N:4]([C:13]([C:15]1[CH:16]=[N:17][N:18]([C:20]2[CH:25]=[CH:24][C:23]([O:26][CH2:27][CH2:28][CH2:29][N:30]3[CH2:34][CH2:33][CH2:32][C@H:31]3[CH3:35])=[CH:22][CH:21]=2)[CH:19]=1)=[O:14])[CH2:5][C:6]([OH:8])=[O:7]

Participants

5

Procedure

To a solution of tert-butyl N-(2-hydroxyethyl)-N-{[1-(4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1H-pyrazol-4-yl]carbonyl}glycinate prepared in Example 67-(3) (0.218 g) in 1,4-dioxane (4.0 ml), a solution of hydrochloric acid in ethyl acetate (4 M, 4.0 ml) was added and stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and the resulting residue was purified by octadecylsilyl (ODS) column chromatography (eluting solvent: acetonitrile:water=95:5) to give the titled compound (0.075 g) as a colorless amorphous substance.

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe resulting residue was purified by octadecylsilyl (ODS) column chromatography (eluting solvent: acetonitrile:water=95:5)

Sources & evidence

ORD record
ord-64021199827e4be9978e2c848f412d5e
Source dataset
uspto-grants-2012_06
Patent number
US08193176B2

Reaction notes

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