Lithium Hydroxide → HCID 22647483, compound

HRID 394359Notes

Reaction equation

HRID 394359 reaction equation
C([O:3][C:4](=[O:33])[CH:5]([O:30][CH2:31][CH3:32])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH2:15][C:16]2[S:20][C:19]([C:21]3[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=3)=[N:18][C:17]=2[CH3:28])=[CH:9][C:8]=1[CH3:29])C.[Li+].[OH-]>>[Cl:27][C:24]1[CH:25]=[CH:26][C:21]([C:19]2[S:20][C:16]([CH2:15][CH2:14][O:13][C:10]3[CH:11]=[CH:12][C:7]([CH2:6][CH:5]([O:30][CH2:31][CH3:32])[C:4]([OH:33])=[O:3])=[C:8]([CH3:29])[CH:9]=3)=[C:17]([CH3:28])[N:18]=2)=[CH:22][CH:23]=1

Participants

3

Procedure

In analogy to the procedure described in example 10 d], [rac]-3-(4-{2-[2-(4-chloro-phenyl)-4-methyl-thiazol-5-yl]-ethoxy}-2-methyl-phenyl)-2-ethoxy-propionic acid ethyl ester was treated with LiOH to obtain [rac]-3-(4-{2-[2-(4-chloro-phenyl)-4-methyl-thiazol-5-yl]-ethoxy}-2-methyl-phenyl)-2-ethoxy-propionic acid as light yellow solid.

Workup

  1. customdescribed in example 10 d

Sources & evidence

ORD record
ord-733296a56f85428187a0a0a82fe81758
Source dataset
uspto-grants-2004_10
Patent number
US06809110B2

Reaction notes

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