Hydrochloric Acid → HCID 10001646, compound

HRID 2212163Notes

Reaction equation

HRID 2212163 reaction equation
[C:1]([O:4][CH2:5][C:6]1[N:7]([CH2:28][C:29]2[CH:34]=[CH:33][C:32]([CH3:35])=[CH:31][CH:30]=2)[C:8]2[C:13]([C:14]=1[C:15](=[O:19])C(O)=O)=[CH:12][C:11]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[CH:10][CH:9]=2)(=[O:3])C.[OH-].[K+].Cl>>[CH2:21]([O:20][C:11]1[CH:12]=[C:13]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:28][C:29]1[CH:30]=[CH:31][C:32]([CH3:35])=[CH:33][CH:34]=1)[C:6]1[CH2:5][O:4][C:1](=[O:3])[C:15](=[O:19])[C:14]2=1)[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1

Participants

4

Procedure

The title compound was prepared from [2-[(acetyloxy)methyl]-5-(benzyloxy)-1-(4-methylbenzyl)-1H-indol-3-yl](oxo)acetic acid and aqueous potassium hydroxide according to the procedure described in step 6 of Example 1, followed by the treatment with aqueous HCl in substantially the same manner, as described in step 7 of Example 1. The product was obtained as an off-white solid; mp: 206–207° C.

Workup

  1. customThe product was obtained as an off-white solid

Sources & evidence

ORD record
ord-09858d41be7d4cba9b22f2271729ca61
Source dataset
uspto-grants-2006_09
Patent number
US07101903B2

Reaction notes

Loading…