(Naphthalen-2-yl)boronic acid → 5-(4-Isopropoxyphenyl)-1-(2-naphthyl)indole-2-carboxylic acid

HRID 646113Notes

Reaction equation

HRID 646113 reaction equation
C([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([C:15]1[CH:20]=[CH:19][C:18]([O:21][CH:22]([CH3:24])[CH3:23])=[CH:17][CH:16]=1)=[CH:10][CH:9]=2)=[O:5])C.[CH:25]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=[CH:27][C:26]=1B(O)O>>[CH:22]([O:21][C:18]1[CH:17]=[CH:16][C:15]([C:11]2[CH:12]=[C:13]3[C:8](=[CH:9][CH:10]=2)[N:7]([C:27]2[CH:26]=[CH:25][C:34]4[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=4)[CH:28]=2)[C:6]([C:4]([OH:3])=[O:5])=[CH:14]3)=[CH:20][CH:19]=1)([CH3:23])[CH3:24]

Participants

3

Reactant 2

HCID 2734375(Naphthalen-2-yl)boronic acidHCID 68696575HCID 68696575, compound

Product 1

HCID 686968775-(4-Isopropoxyphenyl)-1-(2-naphthyl)indole-2-carboxylic acid

Procedure

The title compound was prepared in accordance with Example 8(c) from 5-(4-isopropoxyphenyl)indole-2-carboxylic acid ethyl ester (see step (a) above) and 2-naphthylboronic acid followed by hydrolysis in accordance with the procedure described in Example 1(c).

Workup

  1. customfollowed by hydrolysis in accordance with the procedure

Sources & evidence

ORD record
ord-bde1704c8c414f91b106764f0f365381
Source dataset
uspto-grants-2010_04
Patent number
US07705023B2

Reaction notes

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