HCID 309016, compound → HCID 22123283, compound

HRID 1859204Notes

Reaction equation

HRID 1859204 reaction equation
Br[CH2:2][C:3]1[CH:4]=[C:5]([CH:18]=[CH:19][CH:20]=1)[CH2:6][N:7]1[C:15](=[O:16])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]1=[O:17].[C:21]([CH2:24][C:25]1[CH:26]=[C:27]2[C:31](=[CH:32][CH:33]=1)[NH:30][CH:29]=[CH:28]2)([OH:23])=[O:22]>>[C:21]([CH2:24][C:25]1[CH:26]=[C:27]2[C:31](=[CH:32][CH:33]=1)[N:30]([CH2:2][C:3]1[CH:4]=[C:5]([CH:18]=[CH:19][CH:20]=1)[CH2:6][N:7]1[C:15](=[O:16])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8]1=[O:17])[CH:29]=[CH:28]2)([OH:23])=[O:22]

Participants

3

Procedure

This compound was prepared in a manner analogous to Example 14a) starting from 2-(3-bromomethyl-benzyl)-isoindol-1,3-dione and 5-carboxymethyl-indole.

Workup

  1. customThis compound was prepared in a manner analogous to Example 14a)

Sources & evidence

ORD record
ord-a45936755ec54c559af3312ed0088f0d
Source dataset
uspto-grants-2000_11
Patent number
US06153641

Reaction notes

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