Phenylboronic Acid → HCID 18373328, compound

HRID 2301664Notes

Reaction equation

HRID 2301664 reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH:6]=[C:5]2[CH2:18][C:19]([OH:21])=[O:20].[C:22]1(B(O)O)[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>>[CH2:11]([N:7]1[C:8]2[C:4](=[CH:3][C:2]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[CH:10][CH:9]=2)[C:5]([CH2:18][C:19]([OH:21])=[O:20])=[CH:6]1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 18373270HCID 18373270, compound

Product 1

HCID 18373328HCID 18373328, compound

Procedure

The title compound was prepared according to the procedure described in Example 78 except that 2-[5-bromo-1-benzyl-1H-indol-3-yl]acetic acid and phenylboronic acid were used.

Sources & evidence

ORD record
ord-fba4ac1d0b434d2e951c976852c03a03
Source dataset
uspto-grants-2002_12
Patent number
US06500853B1

Reaction notes

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