Lithium Hydroxide → (2S,4R)-4-(2-Chloro-4-fluorophenylsulfonyl)-1-(3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl)pyrrolidine-2-carboxylic Acid

HRID 1697742Notes

Reaction equation

HRID 1697742 reaction equation
C[O:2][C:3]([C@@H:5]1[CH2:9][C@@H:8]([S:10]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=2[Cl:20])(=[O:12])=[O:11])[CH2:7][N:6]1[C:21]1[N:25]([CH:26]2[CH2:31][CH2:30][O:29][CH2:28][CH2:27]2)[N:24]=[C:23]([CH3:32])[CH:22]=1)=[O:4].[OH-].[Li+]>>[Cl:20][C:14]1[CH:15]=[C:16]([F:19])[CH:17]=[CH:18][C:13]=1[S:10]([C@H:8]1[CH2:7][N:6]([C:21]2[N:25]([CH:26]3[CH2:31][CH2:30][O:29][CH2:28][CH2:27]3)[N:24]=[C:23]([CH3:32])[CH:22]=2)[C@H:5]([C:3]([OH:4])=[O:2])[CH2:9]1)(=[O:12])=[O:11]

Participants

3

Procedure

In analogy to the procedure described in example 253e, (2S,4R)-4-(2-chloro-4-fluorophenylsulfonyl)-1-(3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl)pyrrolidine-2-carboxylic acid methyl ester was saponified in the presence of lithium hydroxide to give the title compound as yellow foam which was used in the next step without further purification. MS (ESI): m/z=472.1 [M+H]+.

Sources & evidence

ORD record
ord-14e72ba281af43fda9e1edae91a62bdd
Source dataset
uspto-grants-2012_04
Patent number
US08163793B2

Reaction notes

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