Sodium Hydroxide → HCID 10099467, compound

HRID 1859910Notes

Reaction equation

HRID 1859910 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:43]=[CH:42][C:10]([C:11]([NH:13][CH2:14][CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]([CH2:23][CH:24]([O:30][C:31]3[CH:36]=[CH:35][C:34]([O:37][C:38]([F:41])([F:40])[F:39])=[CH:33][CH:32]=3)[C:25]([O:27]CC)=[O:26])=[CH:19][CH:18]=2)=[O:12])=[CH:9][CH:8]=1.[OH-].[Na+]>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:43]=[CH:42][C:10]([C:11]([NH:13][CH2:14][CH2:15][O:16][C:17]2[CH:18]=[CH:19][C:20]([CH2:23][CH:24]([O:30][C:31]3[CH:32]=[CH:33][C:34]([O:37][C:38]([F:39])([F:40])[F:41])=[CH:35][CH:36]=3)[C:25]([OH:27])=[O:26])=[CH:21][CH:22]=2)=[O:12])=[CH:9][CH:8]=1

Participants

3

Procedure

In a similar manner to that described in Example 2, ethyl 3-[4-[2-(4-pyridine-2-ylbenzoylamino)ethoxy]phenyl]-2-(4-trifluoromethoxyphenoxy)propionate (1.65 g), which is the product of Example 126, was reacted with aqueous sodium hydroxide solution (1N, 5.54 ml) and the reaction mixture was treated to give the title compound (1.33 g) as colorless crystals.

Workup

  1. additionthe reaction mixture was treated

Sources & evidence

ORD record
ord-2c43c984c2e447ed91c77544eda5f510
Source dataset
uspto-grants-2003_03
Patent number
US06528525B1

Reaction notes

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