Chloride → HCID 21472226, compound

HRID 2294883Notes

Reaction equation

HRID 2294883 reaction equation
[Cl-].[O:2]([CH:9]([CH3:13])[C:10]([OH:12])=O)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH3:14][O:15][C:16]1[CH:28]=[CH:27][C:19]([CH2:20][N:21]2[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]2)=[CH:18][CH:17]=1>>[O:2]([CH:9]([CH3:13])[C:10]([N:24]1[CH2:23][CH2:22][N:21]([CH2:20][C:19]2[CH:27]=[CH:28][C:16]([O:15][CH3:14])=[CH:17][CH:18]=2)[CH2:26][CH2:25]1)=[O:12])[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1

Participants

4

Procedure

By carrying out the preparation as in Example 12 (Stage A), but using the chloride of 2-phenoxypropionic acid and 1-(4-methoxybenzyl)piperazine, the title product is obtained.

Workup

  1. customthe preparation as in Example 12 (Stage A)

Sources & evidence

ORD record
ord-4cd46fc296744bac925702e9f88b892b
Source dataset
uspto-grants-1997_11
Patent number
US05691340

Reaction notes

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