(Naphthalen-2-yl)boronic acid → HCID 22048861, compound

HRID 2087648Notes

Reaction equation

HRID 2087648 reaction equation
Br[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2.[CH:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:14]=[CH:13][C:12]=1B(O)O>>[CH:19]1[C:20]2[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:16]=[CH:17][C:18]=1[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2

Participants

3

Reactant 2

HCID 2734375(Naphthalen-2-yl)boronic acidHCID 27570207-Bromoindole

Product 1

HCID 22048861HCID 22048861, compound

Procedure

Prepared by Procedure I and Scheme T using 7-bromo-1H-indole and 2-naphthylboronic acid: ESMS m/e: 244.0 (M+H)+.

Workup

  1. customPrepared by Procedure I and Scheme T

Sources & evidence

ORD record
ord-60c3798877924a009e68041ee986fb48
Source dataset
uspto-grants-2004_04
Patent number
US06727264B1

Reaction notes

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